nsv4375253
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:303,845
- 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: 1621 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 1623 SVs from 39 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4375253 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 20,052,600 | 20,356,444 |
| nsv4375253 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 22,214,486 | 22,518,330 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15615039 | Remapped | Perfect | NC_000024.10:g.(?_ 20052600)_(2035644 4_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 20,052,600 | 20,356,444 |
| nssv15670363 | Remapped | Perfect | NC_000024.10:g.(?_ 20052600)_(2035644 4_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 20,052,600 | 20,356,444 |
| nssv15615039 | Submitted genomic | NC_000024.9:g.(?_2 2214486)_(22518330 _?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 22,214,486 | 22,518,330 | ||
| nssv15670363 | Submitted genomic | NC_000024.9:g.(?_2 2214486)_(22518330 _?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 22,214,486 | 22,518,330 |