esv2421597
- Organism: Homo sapiens
- Study:estd195 (Altshuler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:32
- Validation:Not tested
- Clinical Assertions: No
- Region Size:24,790
- Publication(s):International HapMap 3 Consortium et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 434 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 434 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 177 SVs from 19 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421597 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| esv2421597 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| esv2421597 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv5019035 | deletion | NA11920 | SNP array | SNP genotyping analysis | 1 | 121 |
| essv5019360 | deletion | NA19779 | SNP array | SNP genotyping analysis | 1 | 124 |
| essv5026356 | deletion | NA18630 | SNP array | SNP genotyping analysis | 1 | 133 |
| essv5028866 | deletion | NA20527 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5035134 | deletion | NA11894 | SNP array | SNP genotyping analysis | 1 | 122 |
| essv5035694 | deletion | NA19661 | SNP array | SNP genotyping analysis | 0 | 144 |
| essv5039745 | deletion | NA19685 | SNP array | SNP genotyping analysis | 1 | 132 |
| essv5052716 | deletion | NA19748 | SNP array | SNP genotyping analysis | 1 | 136 |
| essv5053196 | deletion | NA20755 | SNP array | SNP genotyping analysis | 1 | 130 |
| essv5055902 | deletion | NA19679 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5056585 | deletion | NA20849 | SNP array | SNP genotyping analysis | 1 | 152 |
| essv5058833 | deletion | NA18107 | SNP array | SNP genotyping analysis | 1 | 121 |
| essv5063223 | deletion | NA19746 | SNP array | SNP genotyping analysis | 1 | 136 |
| essv5063233 | deletion | NA20758 | SNP array | SNP genotyping analysis | 1 | 123 |
| essv5068729 | deletion | NA18135 | SNP array | SNP genotyping analysis | 1 | 134 |
| essv5071724 | deletion | NA19662 | SNP array | SNP genotyping analysis | 1 | 118 |
| essv5080934 | deletion | NA12761 | SNP array | SNP genotyping analysis | 1 | 133 |
| essv5081865 | deletion | NA18536 | SNP array | SNP genotyping analysis | 1 | 118 |
| essv5082721 | deletion | NA19650 | SNP array | SNP genotyping analysis | 1 | 133 |
| essv5083361 | deletion | NA20800 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5093779 | deletion | NA20528 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5095832 | deletion | NA20317 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5097776 | deletion | NA19007 | SNP array | SNP genotyping analysis | 1 | 123 |
| essv5106389 | deletion | NA20904 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5106455 | deletion | NA20775 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5107897 | deletion | NA10853 | SNP array | SNP genotyping analysis | 1 | 140 |
| essv5123869 | deletion | NA20778 | SNP array | SNP genotyping analysis | 1 | 123 |
| essv5125436 | deletion | NA12752 | SNP array | SNP genotyping analysis | 1 | 144 |
| essv5130412 | deletion | NA20774 | SNP array | SNP genotyping analysis | 1 | 132 |
| essv5145300 | deletion | NA19818 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5147591 | deletion | NA20810 | SNP array | SNP genotyping analysis | 1 | 127 |
| essv5153993 | deletion | NA11843 | SNP array | SNP genotyping analysis | 1 | 129 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5019035 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5019360 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5026356 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5028866 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5035134 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5035694 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5039745 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5052716 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5053196 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5055902 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5056585 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5058833 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5063223 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5063233 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5068729 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5071724 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5080934 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5081865 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5082721 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5083361 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5093779 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5095832 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5097776 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5106389 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5106455 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5107897 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5123869 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5125436 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5130412 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5145300 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5147591 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5153993 | Remapped | Perfect | NC_000003.12:g.(?_ 89345442)_(8937023 1_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 89,345,442 | 89,370,231 |
| essv5019035 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5019360 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5026356 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5028866 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5035134 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5035694 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5039745 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5052716 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5053196 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5055902 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5056585 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5058833 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5063223 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5063233 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5068729 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5071724 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5080934 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5081865 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5082721 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5083361 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5093779 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5095832 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5097776 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5106389 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5106455 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5107897 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5123869 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5125436 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5130412 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5145300 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5147591 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5153993 | Remapped | Perfect | NC_000003.11:g.(?_ 89394592)_(8941938 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 89,394,592 | 89,419,381 |
| essv5019035 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5019360 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5026356 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5028866 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5035134 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5035694 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5039745 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5052716 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5053196 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5055902 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5056585 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5058833 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5063223 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5063233 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5068729 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5071724 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5080934 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5081865 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5082721 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5083361 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5093779 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5095832 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5097776 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5106389 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5106455 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5107897 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5123869 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5125436 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5130412 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5145300 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5147591 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 | ||
| essv5153993 | Submitted genomic | NC_000003.10:g.(?_ 89477282)_(8950207 1_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 89,477,282 | 89,502,071 |