nsv6314786
- 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:14,753,088
- 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: 25718 SVs from 101 studies. See in: genome view
Overlapping variant regions from other studies: 25743 SVs from 101 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6314786 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 2,877,173 | 17,630,260 |
| nsv6314786 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 2,795,214 | 17,648,380 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17976206 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv17976206 | Remapped | Good | NC_000023.11:g.(28 77173_?)_(?_176302 60)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 2,877,173 | 17,630,260 |
| nssv17976206 | Submitted genomic | NC_000023.10:g.(27 95214_?)_(?_176483 80)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 2,795,214 | 17,648,380 |