nsv984640
- 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:2,671,731
- 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: 7501 SVs from 125 studies. See in: genome view
Overlapping variant regions from other studies: 7543 SVs from 125 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984640 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 27,414,378 | 30,086,108 |
| nsv984640 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 27,659,524 | 30,378,311 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv3217254 | copy number gain | ULSAM449 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3217254 | Remapped | Good | NC_000015.10:g.(?_ 27414378)_(3008610 8_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 27,414,378 | 30,086,108 |
| nssv3217254 | Submitted genomic | NC_000015.9:g.(?_2 7659524)_(30378311 _?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 27,659,524 | 30,378,311 |