nsv7099267
- 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:475,423
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: 1414 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1417 SVs from 88 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7099267 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 232,067,274 | 232,542,696 |
| nsv7099267 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 232,203,020 | 232,678,442 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18793028 | duplication | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18793028 | Remapped | Perfect | NC_000001.11:g.(23 2067274_?)_(?_2325 42696)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 232,067,274 | 232,542,696 |
| nssv18793028 | Submitted genomic | NC_000001.10:g.(23 2203020_?)_(?_2326 78442)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 232,203,020 | 232,678,442 |