nsv984592
- Organism: Homo sapiens
- Study:nstd92 (Forsberg et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:82,081,602
- Publication(s):Forsberg et al. 2014
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: 231258 SVs from 157 studies. See in: genome view
Overlapping variant regions from other studies: 231284 SVs from 157 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984592 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 19,898,947 | 101,980,548 |
| nsv984592 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 20,104,200 | 102,520,751 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv3217252 | copy number gain | ULSAM432 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3217252 | Remapped | Good | NC_000015.10:g.(?_ 19898947)_(1019805 48_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 19,898,947 | 101,980,548 |
| nssv3217252 | Submitted genomic | NC_000015.9:g.(?_2 0104200)_(10252075 1_?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 20,104,200 | 102,520,751 |