nsv4365710
- 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:469,523
- 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: 2006 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 1875 SVs from 55 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4365710 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 1,907,633 | 2,377,155 |
| nsv4365710 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 2,026,526 | 2,295,196 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15629745 | copy number gain | 1-0574-003 | SNP array | Genotyping | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15629745 | Remapped | Pass | NC_000023.11:g.(?_ 1907633)_(2377155_ ?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 1,907,633 | 2,377,155 |
| nssv15629745 | Submitted genomic | NC_000023.10:g.(?_ 2026526)_(2295196_ ?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 2,026,526 | 2,295,196 |