nsv433191
- Organism: Homo sapiens
- Study:nstd14 (Cooper 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:48,079
- Publication(s):Cooper 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: 1464 SVs from 100 studies. See in: genome view
Overlapping variant regions from other studies: 1464 SVs from 100 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433191 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 196,753,917 | 196,801,995 |
| nsv433191 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 196,723,047 | 196,771,125 |
| nsv433191 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 193,454,704 | 193,502,782 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463072 | Remapped | Perfect | NC_000001.11:g.(?_ 196753917)_(196801 995_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 196,753,917 | 196,801,995 |
| nssv463072 | Remapped | Perfect | NC_000001.10:g.(?_ 196723047)_(196771 125_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 196,723,047 | 196,771,125 |
| nssv463072 | Submitted genomic | NC_000001.8:g.(?_1 93454704)_(1935027 82_?)del | NCBI35 (hg17) | NC_000001.8 | Chr1 | 193,454,704 | 193,502,782 |