nsv828041
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:156,944
- Publication(s):Park et al. 2010
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: 504 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 503 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 139 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv828041 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 51,902,161 | 52,059,104 |
| nsv828041 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 49,979,521 | 50,136,464 |
| nsv828041 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 47,334,520 | 47,491,463 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421542 | Remapped | Perfect | NC_000017.11:g.(?_ 51902161)_(5205910 4_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 51,902,161 | 52,059,104 |
| nssv1421542 | Remapped | Perfect | NC_000017.10:g.(?_ 49979521)_(5013646 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 49,979,521 | 50,136,464 |
| nssv1421542 | Submitted genomic | NC_000017.9:g.(?_4 7334520)_(47491463 _?)del | NCBI36 (hg18) | NC_000017.9 | Chr17 | 47,334,520 | 47,491,463 |