nsv824847
- 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:122,640
- 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: 758 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 762 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 335 SVs from 22 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 |
---|---|---|---|---|---|---|---|---|---|
nsv824847 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 9,255,377 | 9,378,016 |
nsv824847 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 9,255,377 | 9,378,016 |
nsv824847 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 9,245,377 | 9,368,016 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1438976 | Remapped | Perfect | NC_000009.12:g.(?_ 9255377)_(9378016_ ?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 9,255,377 | 9,378,016 |
nssv1438976 | Remapped | Perfect | NC_000009.11:g.(?_ 9255377)_(9378016_ ?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 9,255,377 | 9,378,016 |
nssv1438976 | Submitted genomic | NC_000009.10:g.(?_ 9245377)_(9368016_ ?)del | NCBI36 (hg18) | NC_000009.10 | Chr9 | 9,245,377 | 9,368,016 |