nsv827390
- 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:29,284
- 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: 299 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 299 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv827390 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 75,473,746 | 75,503,029 |
| nsv827390 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 75,766,087 | 75,795,370 |
| nsv827390 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 73,553,140 | 73,582,425 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1441512 | Remapped | Good | NC_000015.10:g.(?_ 75473746)_(7550302 9_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 75,473,746 | 75,503,029 |
| nssv1441512 | Remapped | Good | NC_000015.9:g.(?_7 5766087)_(75795370 _?)dup | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 75,766,087 | 75,795,370 |
| nssv1441512 | Submitted genomic | NC_000015.8:g.(?_7 3553140)_(73582425 _?)dup | NCBI36 (hg18) | NC_000015.8 | Chr15 | 73,553,140 | 73,582,425 |