nsv4423955
- 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:378,818
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1174 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1174 SVs from 85 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4423955 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 45,956,714 | 45,978,684 | 46,264,600 | 46,335,531 |
| nsv4423955 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 46,425,917 | 46,447,887 | 46,733,803 | 46,804,734 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15721592 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15721592 | Remapped | Perfect | NC_000014.9:g.(459 56714_45978684)_(4 6264600_46335531)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 45,956,714 | 45,978,684 | 46,264,600 | 46,335,531 |
| nssv15721592 | Submitted genomic | NC_000014.8:g.(464 25917_46447887)_(4 6733803_46804734)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 46,425,917 | 46,447,887 | 46,733,803 | 46,804,734 |