nsv4376591
- 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:42,446
- 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: 480 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 481 SVs from 35 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4376591 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 30,060,525 | 30,102,970 |
| nsv4376591 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 30,078,642 | 30,121,087 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15682229 | copy number loss | 222684 | SNP array | Genotyping | 25 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15682229 | Remapped | Perfect | NC_000023.11:g.(?_ 30060525)_(3010297 0_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 30,060,525 | 30,102,970 |
| nssv15682229 | Submitted genomic | NC_000023.10:g.(?_ 30078642)_(3012108 7_?)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 30,078,642 | 30,121,087 |