nsv2751775
- Organism: Homo sapiens
- Study:nstd130 (Leppa et al. 2016)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,468,001
- Publication(s):Leppa et al. 2016
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: 2600 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 3056 SVs from 81 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2751775 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 35,997,947 | 46,465,947 |
| nsv2751775 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 35,232,318 | 46,499,859 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv13612505 | deletion | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv13612505 | Remapped | Pass | NC_000016.10:g.(?_ 35997947)_(4646594 7_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,997,947 | 46,465,947 |
| nssv13612505 | Submitted genomic | NC_000016.9:g.(?_3 5232318)_(46499859 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 35,232,318 | 46,499,859 |