nsv4410979
- 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:440,853
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1108 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 1108 SVs from 72 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4410979 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 61,776,757 | 61,776,757 | 62,217,177 | 62,217,609 |
| nsv4410979 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 62,486,662 | 62,486,662 | 62,927,082 | 62,927,514 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15738538 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15738538 | Remapped | Perfect | NC_000006.12:g.(61 776757_61776757)_( 62217177_62217609) del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 61,776,757 | 61,776,757 | 62,217,177 | 62,217,609 |
| nssv15738538 | Submitted genomic | NC_000006.11:g.(62 486662_62486662)_( 62927082_62927514) del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 62,486,662 | 62,486,662 | 62,927,082 | 62,927,514 |