nsv6136791
- Organism: Homo sapiens
- Study:nstd213 (Pham et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:73,208,756
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: 103866 SVs from 107 studies. See in: genome view
Overlapping variant regions from other studies: 103959 SVs from 107 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6136791 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 62,510,530 | 135,719,285 |
| nsv6136791 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 61,730,000 | 134,860,001 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17679534 | copy number loss | SAMN20524661 | Sequencing | Paired-end mapping | 62 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17679534 | Remapped | Good | NC_000023.11:g.625 10530_135719285del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 62,510,530 | 135,719,285 |
| nssv17679534 | Submitted genomic | NC_000023.10:g.617 30000_134860001del | GRCh37 (hg19) | NC_000023.10 | ChrX | 61,730,000 | 134,860,001 |