nsv3961964
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:copy number variation
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:309,136
- Publication(s):Levy-Sakin et al. 2019
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: 167 SVs from 41 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|
nsv3961964 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 67,920,453 | 68,229,588 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15209410 | deletion | Optical mapping | Optical mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|
nssv15209410 | Submitted genomic | NC_000009.12:g.(67 920453_?)_(?_68229 588)del | GRCh38 (hg38) | NC_000009.12 | Chr9 | 67,920,453 | 68,229,588 |