nsv822323
- 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:94,441
- 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: 499 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 499 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 204 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv822323 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 163,135,241 | 163,229,681 |
| nsv822323 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 162,853,029 | 162,947,469 |
| nsv822323 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 164,335,723 | 164,430,163 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1425097 | Remapped | Perfect | NC_000003.12:g.(?_ 163135241)_(163229 681_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 163,135,241 | 163,229,681 |
| nssv1425097 | Remapped | Perfect | NC_000003.11:g.(?_ 162853029)_(162947 469_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 162,853,029 | 162,947,469 |
| nssv1425097 | Submitted genomic | NC_000003.10:g.(?_ 164335723)_(164430 163_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 164,335,723 | 164,430,163 |