nsv6627508
- 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:34,914
- 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: 188 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 188 SVs from 39 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6627508 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 120,764,444 | 120,799,357 |
| nsv6627508 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 121,522,020 | 121,556,933 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18310886 | Remapped | Perfect | NC_000002.12:g.(?_ 120764444)_(120799 357_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 120,764,444 | 120,799,357 |
| nssv18313929 | Remapped | Perfect | NC_000002.12:g.(?_ 120764444)_(120799 357_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 120,764,444 | 120,799,357 |
| nssv18310886 | Submitted genomic | NC_000002.11:g.(?_ 121522020)_(121556 933_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 121,522,020 | 121,556,933 | ||
| nssv18313929 | Submitted genomic | NC_000002.11:g.(?_ 121522020)_(121556 933_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 121,522,020 | 121,556,933 |