nsv4422261
- 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:206,875
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 595 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 595 SVs from 64 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4422261 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 73,715,689 | 73,715,689 | 73,922,563 | 73,922,563 |
| nsv4422261 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 75,475,447 | 75,475,447 | 75,682,321 | 75,682,321 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15708423 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15708423 | Remapped | Perfect | NC_000010.11:g.(73 715689_73715689)_( 73922563_73922563) dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 73,715,689 | 73,715,689 | 73,922,563 | 73,922,563 |
| nssv15708423 | Submitted genomic | NC_000010.10:g.(75 475447_75475447)_( 75682321_75682321) dup | GRCh37 (hg19) | NC_000010.10 | Chr10 | 75,475,447 | 75,475,447 | 75,682,321 | 75,682,321 |