nsv984814
- Organism: Homo sapiens
- Study:nstd92 (Forsberg et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:54,061,423
- Publication(s):Forsberg et al. 2014
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: 17260 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 17325 SVs from 76 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984814 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 2,826,480 | 56,887,902 |
| nsv984814 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 2,694,521 | 59,034,049 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv3217225 | copy number loss | ULSAM223 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3217225 | Remapped | Good | NC_000024.10:g.(?_ 2826480)_(56887902 _?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 2,826,480 | 56,887,902 |
| nssv3217225 | Submitted genomic | NC_000024.9:g.(?_2 694521)_(59034049_ ?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 2,694,521 | 59,034,049 |