nsv433190
- 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:74,409
- 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: 606 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 606 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433190 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 189,737,495 | 189,811,903 |
| nsv433190 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 189,706,625 | 189,781,033 |
| nsv433190 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 186,438,282 | 186,512,690 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463071 | Remapped | Perfect | NC_000001.11:g.(?_ 189737495)_(189811 903_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,737,495 | 189,811,903 |
| nssv463071 | Remapped | Perfect | NC_000001.10:g.(?_ 189706625)_(189781 033_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,706,625 | 189,781,033 |
| nssv463071 | Submitted genomic | NC_000001.8:g.(?_1 86438282)_(1865126 90_?)del | NCBI35 (hg17) | NC_000001.8 | Chr1 | 186,438,282 | 186,512,690 |