nsv4378527
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:142,939
- Publication(s):Zarrei et al. 2019
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: 1967 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1967 SVs from 96 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4378527 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 24,105,709 | 24,248,647 |
| nsv4378527 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 24,350,856 | 24,493,794 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15642009 | copy number loss | 15-1127-004 | SNP array | Genotyping | 32 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15642009 | Remapped | Perfect | NC_000015.10:g.(?_ 24105709)_(2424864 7_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 24,105,709 | 24,248,647 |
| nssv15642009 | Submitted genomic | NC_000015.9:g.(?_2 4350856)_(24493794 _?)del | GRCh37 (hg19) | NC_000015.9 | Chr15 | 24,350,856 | 24,493,794 |