nsv6634149
- Organism: Homo sapiens
- Study:nstd224 (Zarrei 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:135,506
- Publication(s):Zarrei et al. 2023
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: 683 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 688 SVs from 67 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6634149 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 47,977,713 | 48,113,218 |
| nsv6634149 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 47,837,112 | 47,972,601 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18286073 | deletion | OSC2794 | SNP array | Probe signal intensity | nssv18285483, nssv18285694, nssv18286072 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18286073 | Remapped | Good | NC_000023.11:g.(?_ 47977713)_(4811321 8_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 47,977,713 | 48,113,218 |
| nssv18286073 | Submitted genomic | NC_000023.10:g.(?_ 47837112)_(4797260 1_?)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 47,837,112 | 47,972,601 |