nsv433423
- 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:5,849
- 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: 156 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 156 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 10 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433423 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 21,581,164 | 21,587,012 |
| nsv433423 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 22,049,298 | 22,055,136 |
| nsv433423 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000014.7 | Chr14 | 21,119,138 | 21,124,976 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463304 | Remapped | Good | NC_000014.9:g.(?_2 1581164)_(21587012 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 21,581,164 | 21,587,012 |
| nssv463304 | Remapped | Perfect | NC_000014.8:g.(?_2 2049298)_(22055136 _?)dup | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 22,049,298 | 22,055,136 |
| nssv463304 | Submitted genomic | NC_000014.7:g.(?_2 1119138)_(21124976 _?)dup | NCBI35 (hg17) | NC_000014.7 | Chr14 | 21,119,138 | 21,124,976 |