nsv4383389
- 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:12,476,687
- 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: 42779 SVs from 150 studies. See in: genome view
Overlapping variant regions from other studies: 43752 SVs from 151 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4383389 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 21,111,373 | 33,588,059 |
| nsv4383389 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 21,465,662 | 33,984,045 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15680985 | copy number gain | 181225 | SNP array | Genotyping | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15680985 | Remapped | Good | NC_000022.11:g.(?_ 21111373)_(3358805 9_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 21,111,373 | 33,588,059 |
| nssv15680985 | Submitted genomic | NC_000022.10:g.(?_ 21465662)_(3398404 5_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 21,465,662 | 33,984,045 |