nsv821473
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:27,512
- Publication(s):Ju 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: 1589 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 1589 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 740 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821473 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 24,240,456 | 24,267,967 |
| nsv821473 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 24,485,603 | 24,513,114 |
| nsv821473 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 22,036,696 | 22,064,207 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421111 | Remapped | Perfect | NC_000015.10:g.(?_ 24240456)_(2426796 7_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 24,240,456 | 24,267,967 |
| nssv1421111 | Remapped | Perfect | NC_000015.9:g.(?_2 4485603)_(24513114 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 24,485,603 | 24,513,114 |
| nssv1421111 | Submitted genomic | NC_000015.8:g.(?_2 2036696)_(22064207 _?)del | NCBI36 (hg18) | NC_000015.8 | Chr15 | 22,036,696 | 22,064,207 |