nsv6314782
- Organism: Homo sapiens
- Study:nstd220 (Chen et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,896,904
- Publication(s):Chen et al. 2022
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: 14056 SVs from 139 studies. See in: genome view
Overlapping variant regions from other studies: 15001 SVs from 141 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6314782 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 21,351,861 | 24,248,764 |
| nsv6314782 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 21,706,150 | 24,644,732 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17976202 | copy number loss | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17976202 | Remapped | Good | NC_000022.11:g.(21 351861_?)_(?_24248 764)del | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 21,351,861 | 24,248,764 |
| nssv17976202 | Submitted genomic | NC_000022.10:g.(21 706150_?)_(?_24644 732)del | GRCh37 (hg19) | NC_000022.10 | Chr22 | 21,706,150 | 24,644,732 |