nsv4375992
- 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:82,783
- 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: 555 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 556 SVs from 26 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4375992 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 23,378,654 | 23,461,436 |
| nsv4375992 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 25,524,801 | 25,607,583 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15633467 | Remapped | Perfect | NC_000024.10:g.(?_ 23378654)_(2346143 6_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 23,378,654 | 23,461,436 |
| nssv15639460 | Remapped | Perfect | NC_000024.10:g.(?_ 23378654)_(2346143 6_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 23,378,654 | 23,461,436 |
| nssv15633467 | Submitted genomic | NC_000024.9:g.(?_2 5524801)_(25607583 _?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 25,524,801 | 25,607,583 | ||
| nssv15639460 | Submitted genomic | NC_000024.9:g.(?_2 5524801)_(25607583 _?)del | GRCh37 (hg19) | NC_000024.9 | ChrY | 25,524,801 | 25,607,583 |