nsv7099294
- 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:96,398
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: 713 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 713 SVs from 68 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 |
---|---|---|---|---|---|---|---|---|---|
nsv7099294 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 89,327,596 | 89,423,993 |
nsv7099294 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 89,394,004 | 89,490,401 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18793007 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18793007 | Remapped | Perfect | NC_000016.10:g.(89 327596_?)_(?_89423 993)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 89,327,596 | 89,423,993 |
nssv18793007 | Submitted genomic | NC_000016.9:g.(893 94004_?)_(?_894904 01)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 89,394,004 | 89,490,401 |