nsv432256
- Organism: Homo sapiens
- Study:nstd12 (Marshall et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:267,514
- Publication(s):Marshall et al. 2008
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: 3025 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 3026 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 316 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv432256 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 766,831 | 1,034,344 |
| nsv432256 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 727,566 | 995,079 |
| nsv432256 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 697,566 | 965,079 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv565486 | copy number gain | 43734 | SNP array | SNP genotyping analysis | 12 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv565486 | Remapped | Perfect | NC_000023.11:g.(?_ 766831)_(1034344_? )dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 766,831 | 1,034,344 |
| nssv565486 | Remapped | Perfect | NC_000023.10:g.(?_ 727566)_(995079_?) dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 727,566 | 995,079 |
| nssv565486 | Submitted genomic | NC_000023.8:g.(?_6 97566)_(965079_?)d up | NCBI35 (hg17) | NC_000023.8 | ChrX | 697,566 | 965,079 |