nsv824269
- 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:190,675
- 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: 1992 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 1992 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 507 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv824269 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 111,427,973 | 111,618,647 |
| nsv824269 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 111,068,029 | 111,258,703 |
| nsv824269 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 110,855,265 | 111,045,939 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1437524 | Remapped | Perfect | NC_000007.14:g.(?_ 111427973)_(111618 647_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 111,427,973 | 111,618,647 |
| nssv1437524 | Remapped | Perfect | NC_000007.13:g.(?_ 111068029)_(111258 703_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 111,068,029 | 111,258,703 |
| nssv1437524 | Submitted genomic | NC_000007.12:g.(?_ 110855265)_(111045 939_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 110,855,265 | 111,045,939 |