nsv825436
- 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:88,685
- 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: 1460 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 1460 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 352 SVs from 24 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv825436 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 66,560,060 | 66,648,744 |
| nsv825436 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 68,319,818 | 68,408,502 |
| nsv825436 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 67,989,824 | 68,078,508 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1439065 | Remapped | Perfect | NC_000010.11:g.(?_ 66560060)_(6664874 4_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 66,560,060 | 66,648,744 |
| nssv1439065 | Remapped | Perfect | NC_000010.10:g.(?_ 68319818)_(6840850 2_?)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 68,319,818 | 68,408,502 |
| nssv1439065 | Submitted genomic | NC_000010.9:g.(?_6 7989824)_(68078508 _?)del | NCBI36 (hg18) | NC_000010.9 | Chr10 | 67,989,824 | 68,078,508 |