nsv4382761
- 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:323,328
- 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: 2867 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 2864 SVs from 59 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4382761 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 1,615,505 | 1,938,832 |
| nsv4382761 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 1,734,398 | 2,057,725 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15621981 | Remapped | Perfect | NC_000023.11:g.(?_ 1615505)_(1938832_ ?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 1,615,505 | 1,938,832 |
| nssv15632072 | Remapped | Perfect | NC_000023.11:g.(?_ 1615505)_(1938832_ ?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 1,615,505 | 1,938,832 |
| nssv15621981 | Submitted genomic | NC_000023.10:g.(?_ 1734398)_(2057725_ ?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 1,734,398 | 2,057,725 | ||
| nssv15632072 | Submitted genomic | NC_000023.10:g.(?_ 1734398)_(2057725_ ?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 1,734,398 | 2,057,725 |