nsv4426095
- 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:170,272
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 804 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 805 SVs from 68 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4426095 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 30,710,632 | 30,710,632 | 30,880,903 | 30,880,903 |
| nsv4426095 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000021.8 | Chr21 | 32,082,950 | 32,082,954 | 32,246,306 | 32,253,222 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15710915 | copy number gain | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15710915 | Remapped | Good | NC_000021.9:g.(307 10632_30710632)_(3 0880903_30880903)d up | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 30,710,632 | 30,710,632 | 30,880,903 | 30,880,903 |
| nssv15710915 | Submitted genomic | NC_000021.8:g.(320 82950_32082954)_(3 2246306_32253222)d up | GRCh37 (hg19) | NC_000021.8 | Chr21 | 32,082,950 | 32,082,954 | 32,246,306 | 32,253,222 |