nsv7099300
- 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:18,503
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: 314 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 312 SVs from 41 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7099300 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 48,365,020 | 48,383,522 |
| nsv7099300 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 48,224,455 | 48,242,963 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18792936 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18792936 | Remapped | Good | NC_000023.11:g.(48 365020_?)_(?_48383 522)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 48,365,020 | 48,383,522 |
| nssv18792936 | Submitted genomic | NC_000023.10:g.(48 224455_?)_(?_48242 963)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 48,224,455 | 48,242,963 |