nsv7099266
- 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:8,943,222
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: 23464 SVs from 125 studies. See in: genome view
Overlapping variant regions from other studies: 23452 SVs from 125 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7099266 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 226,993,371 | 235,936,592 |
| nsv7099266 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 227,181,072 | 236,099,892 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18792997 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18792997 | Remapped | Good | NC_000001.11:g.(22 6993371_?)_(?_2359 36592)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 226,993,371 | 235,936,592 |
| nssv18792997 | Submitted genomic | NC_000001.10:g.(22 7181072_?)_(?_2360 99892)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 227,181,072 | 236,099,892 |