nsv7099284
- Organism: Homo sapiens
- Study:nstd231 (Ali et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:44,391
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: 176 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 176 SVs from 34 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv7099284 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 34,337,344 | 34,381,734 |
nsv7099284 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 34,626,272 | 34,670,662 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18792933 | deletion | SNP array | SNP genotyping analysis |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18792933 | Remapped | Perfect | NC_000010.11:g.(34 337344_?)_(?_34381 734)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 34,337,344 | 34,381,734 |
nssv18792933 | Submitted genomic | NC_000010.10:g.(34 626272_?)_(?_34670 662)del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 34,626,272 | 34,670,662 |