nsv433455
- 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:35,479
- 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 83 studies. See in: genome view
Overlapping variant regions from other studies: 606 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 28 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433455 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 52,828,661 | 52,864,139 |
| nsv433455 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 53,331,914 | 53,367,392 |
| nsv433455 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000019.8 | Chr19 | 58,023,726 | 58,059,204 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463336 | Remapped | Perfect | NC_000019.10:g.(?_ 52828661)_(5286413 9_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,828,661 | 52,864,139 |
| nssv463336 | Remapped | Perfect | NC_000019.9:g.(?_5 3331914)_(53367392 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,331,914 | 53,367,392 |
| nssv463336 | Submitted genomic | NC_000019.8:g.(?_5 8023726)_(58059204 _?)dup | NCBI35 (hg17) | NC_000019.8 | Chr19 | 58,023,726 | 58,059,204 |