nsv4368051
- 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:3,464,657
- 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: 1785 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 1786 SVs from 55 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4368051 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 2,782,100 | 6,246,756 |
| nsv4368051 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 2,650,141 | 6,114,797 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15664908 | copy number gain | 264923 | SNP array | Genotyping | 28 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15664908 | Remapped | Perfect | NC_000024.10:g.(?_ 2782100)_(6246756_ ?)dup | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 2,782,100 | 6,246,756 |
| nssv15664908 | Submitted genomic | NC_000024.9:g.(?_2 650141)_(6114797_? )dup | GRCh37 (hg19) | NC_000024.9 | ChrY | 2,650,141 | 6,114,797 |