nsv4399968
- 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:880,009
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 3651 SVs from 101 studies. See in: genome view
Overlapping variant regions from other studies: 3679 SVs from 101 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4399968 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 142,055,440 | 142,055,440 | 142,935,448 | 142,935,448 |
| nsv4399968 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 143,136,801 | 143,237,228 | 143,870,232 | 144,016,864 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15743394 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15743394 | Remapped | Good | NC_000008.11:g.(14 2055440_142055440) _(142935448_142935 448)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 142,055,440 | 142,055,440 | 142,935,448 | 142,935,448 |
| nssv15743394 | Submitted genomic | NC_000008.10:g.(14 3136801_143237228) _(143870232_144016 864)del | GRCh37 (hg19) | NC_000008.10 | Chr8 | 143,136,801 | 143,237,228 | 143,870,232 | 144,016,864 |