nsv3115031
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,456
- Publication(s):Lu et al. 2017
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: 142 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 142 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3115031 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 43,464,908 | 43,472,363 |
| nsv3115031 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 42,093,548 | 42,101,003 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14099846 | deletion | sample145 | Oligo aCGH | Probe signal intensity | 103 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14099846 | Remapped | Perfect | NC_000020.11:g.(?_ 43464908)_(4347236 3_?)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 43,464,908 | 43,472,363 |
| nssv14099846 | Submitted genomic | NC_000020.10:g.(?_ 42093548)_(4210100 3_?)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 42,093,548 | 42,101,003 |