nsv482901
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:166,005
- Publication(s):Sharp et al. 2006
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 525 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 525 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv482901 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 81,717,978 | 81,883,982 |
| nsv482901 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 82,010,319 | 82,176,323 |
| nsv482901 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000015.7 | Chr15 | 79,726,138 | 79,892,142 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3010347 | copy number loss | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3010347 | Remapped | Perfect | NC_000015.10:g.(?_ 81717978)_(8188398 2_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 81,717,978 | 81,883,982 |
| nssv3010347 | Remapped | Perfect | NC_000015.9:g.(?_8 2010319)_(82176323 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 82,010,319 | 82,176,323 |
| nssv3010347 | Submitted genomic | NC_000015.7:g.(?_7 9726138)_(79892142 _?)del | NCBI34 (hg16) | NC_000015.7 | Chr15 | 79,726,138 | 79,892,142 |