nsv818486
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:80,493
- Publication(s):Wang et al. 2007
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: 545 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 545 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818486 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 15,039,366 | 15,119,858 |
| nsv818486 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 15,078,991 | 15,159,483 |
| nsv818486 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 14,852,231 | 14,932,723 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416070 | Remapped | Perfect | NC_000007.14:g.(?_ 15039366)_(1511985 8_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 15,039,366 | 15,119,858 |
| nssv1416070 | Remapped | Perfect | NC_000007.13:g.(?_ 15078991)_(1515948 3_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 15,078,991 | 15,159,483 |
| nssv1416070 | Submitted genomic | NC_000007.11:g.(?_ 14852231)_(1493272 3_?)del | NCBI35 (hg17) | NC_000007.11 | Chr7 | 14,852,231 | 14,932,723 |