nsv4428571
- 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:115,918
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 613 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 613 SVs from 77 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4428571 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 130,876,741 | 130,878,727 | 130,978,235 | 130,992,658 |
| nsv4428571 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 133,752,128 | 133,754,114 | 133,853,622 | 133,868,045 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15744753 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15744753 | Remapped | Perfect | NC_000009.12:g.(13 0876741_130878727) _(130978235_130992 658)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 130,876,741 | 130,878,727 | 130,978,235 | 130,992,658 |
| nssv15744753 | Submitted genomic | NC_000009.11:g.(13 3752128_133754114) _(133853622_133868 045)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 133,752,128 | 133,754,114 | 133,853,622 | 133,868,045 |