nsv4415186
- 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:126,138
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 883 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 883 SVs from 80 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4415186 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 43,622,551 | 43,656,668 | 43,748,688 | 43,748,688 |
| nsv4415186 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 43,914,749 | 43,948,866 | 44,040,886 | 44,040,886 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15709286 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15709286 | Remapped | Perfect | NC_000015.10:g.(43 622551_43656668)_( 43748688_43748688) dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 43,622,551 | 43,656,668 | 43,748,688 | 43,748,688 |
| nssv15709286 | Submitted genomic | NC_000015.9:g.(439 14749_43948866)_(4 4040886_44040886)d up | GRCh37 (hg19) | NC_000015.9 | Chr15 | 43,914,749 | 43,948,866 | 44,040,886 | 44,040,886 |