nsv4403143
- 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:4,557
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 114 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 114 SVs from 28 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4403143 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 145,823,291 | 145,823,326 | 145,827,777 | 145,827,847 |
| nsv4403143 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 146,144,427 | 146,144,462 | 146,148,913 | 146,148,983 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15739306 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15739306 | Remapped | Perfect | NC_000006.12:g.(14 5823291_145823326) _(145827777_145827 847)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 145,823,291 | 145,823,326 | 145,827,777 | 145,827,847 |
| nssv15739306 | Submitted genomic | NC_000006.11:g.(14 6144427_146144462) _(146148913_146148 983)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 146,144,427 | 146,144,462 | 146,148,913 | 146,148,983 |