nsv903085
- Organism: Homo sapiens
- Study:nstd71 (Xu et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:573,699
- Publication(s):Xu et al. 2011
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: 5722 SVs from 107 studies. See in: genome view
Overlapping variant regions from other studies: 3006 SVs from 33 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv903085 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 20,924,655 | 21,446,341 | 21,498,353 | - |
| nsv903085 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 19,342,630 | 19,350,081 | 19,503,880 | 19,519,922 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1503268 | copy number gain | SP52019 | SNP array | SNP genotyping analysis | 22 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1503268 | Remapped | Pass | NC_000015.10:g.(20 924655_21446341)_( 21498353_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 20,924,655 | 21,446,341 | 21,498,353 | - |
| nssv1503268 | Submitted genomic | NC_000015.8:g.(193 42630_19350081)_(1 9503880_19519922)d up | NCBI36 (hg18) | NC_000015.8 | Chr15 | 19,342,630 | 19,350,081 | 19,503,880 | 19,519,922 |