nsv4370401
- 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:125,448
- 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: 527 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 528 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4370401 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 25,507,235 | 25,632,682 |
| nsv4370401 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 27,653,382 | 27,778,829 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15639735 | Remapped | Perfect | NC_000024.10:g.(?_ 25507235)_(2563268 2_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 25,507,235 | 25,632,682 |
| nssv15681955 | Remapped | Perfect | NC_000024.10:g.(?_ 25507235)_(2563268 2_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 25,507,235 | 25,632,682 |
| nssv15639735 | Submitted genomic | NC_000024.9:g.(?_2 7653382)_(27778829 _?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 27,653,382 | 27,778,829 | ||
| nssv15681955 | Submitted genomic | NC_000024.9:g.(?_2 7653382)_(27778829 _?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 27,653,382 | 27,778,829 |