nsv4428309
- Organism: Homo sapiens
- Study:nstd174 (DGV Gold Standard)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:300,099
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1576 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1576 SVs from 85 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4428309 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 6,428,897 | 6,456,895 | 6,687,965 | 6,728,995 |
| nsv4428309 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 6,478,898 | 6,506,896 | 6,737,966 | 6,778,996 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15723386 | copy number loss | Multiple | Multiple |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15723386 | Remapped | Perfect | NC_000016.10:g.(64 28897_6456895)_(66 87965_6728995)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 6,428,897 | 6,456,895 | 6,687,965 | 6,728,995 |
| nssv15723386 | Submitted genomic | NC_000016.9:g.(647 8898_6506896)_(673 7966_6778996)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 6,478,898 | 6,506,896 | 6,737,966 | 6,778,996 |