nsv6621306
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:30,605
- Publication(s):Zarrei et al. 2023
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: 1030 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 1031 SVs from 86 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6621306 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 11,061,399 | 11,092,003 |
| nsv6621306 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 11,213,998 | 11,244,602 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18286907 | Remapped | Perfect | NC_000012.12:g.(?_ 11061399)_(1109200 3_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,061,399 | 11,092,003 |
| nssv18293668 | Remapped | Perfect | NC_000012.12:g.(?_ 11061399)_(1109200 3_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,061,399 | 11,092,003 |
| nssv18286907 | Submitted genomic | NC_000012.11:g.(?_ 11213998)_(1124460 2_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,213,998 | 11,244,602 | ||
| nssv18293668 | Submitted genomic | NC_000012.11:g.(?_ 11213998)_(1124460 2_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,213,998 | 11,244,602 |