nsv825813
- 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:64,892
- 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: 425 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 427 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 167 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv825813 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 31,603,380 | 31,668,271 |
| nsv825813 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 31,624,927 | 31,689,819 |
| nsv825813 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 31,581,503 | 31,646,395 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1439124 | Remapped | Good | NC_000011.10:g.(?_ 31603380)_(3166827 1_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 31,603,380 | 31,668,271 |
| nssv1439124 | Remapped | Perfect | NC_000011.9:g.(?_3 1624927)_(31689819 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 31,624,927 | 31,689,819 |
| nssv1439124 | Submitted genomic | NC_000011.8:g.(?_3 1581503)_(31646395 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 31,581,503 | 31,646,395 |