nsv7099298
- 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:13,068,339
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: 31531 SVs from 129 studies. See in: genome view
Overlapping variant regions from other studies: 31533 SVs from 129 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7099298 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 68,115,402 | 81,183,740 |
| nsv7099298 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 68,581,085 | 81,649,425 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18793017 | copy number gain | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18793017 | Remapped | Perfect | NC_000001.11:g.(68 115402_?)_(?_81183 740)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 68,115,402 | 81,183,740 |
| nssv18793017 | Submitted genomic | NC_000001.10:g.(68 581085_?)_(?_81649 425)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 68,581,085 | 81,649,425 |