nsv482869
- 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:166,872
- 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: 506 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 507 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482869 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 17,091,530 | 17,258,401 |
| nsv482869 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 19,203,410 | 19,370,281 |
| nsv482869 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000024.6 | ChrY | 18,148,600 | 18,315,471 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3010191 | copy number gain | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3010191 | Remapped | Perfect | NC_000024.10:g.(?_ 17091530)_(1725840 1_?)dup | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 17,091,530 | 17,258,401 |
| nssv3010191 | Remapped | Perfect | NC_000024.9:g.(?_1 9203410)_(19370281 _?)dup | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 19,203,410 | 19,370,281 |
| nssv3010191 | Submitted genomic | NC_000024.6:g.(?_1 8148600)_(18315471 _?)dup | NCBI34 (hg16) | NC_000024.6 | ChrY | 18,148,600 | 18,315,471 |