nsv4385291
- 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:31,498
- 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: 1112 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 1112 SVs from 69 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4385291 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 14,895,454 | 14,926,951 |
| nsv4385291 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 14,876,100 | 14,907,597 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15651638 | copy number loss | 2-1528-001 | SNP array | Genotyping | 22 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15651638 | Remapped | Perfect | NC_000020.11:g.(?_ 14895454)_(1492695 1_?)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 14,895,454 | 14,926,951 |
| nssv15651638 | Submitted genomic | NC_000020.10:g.(?_ 14876100)_(1490759 7_?)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 14,876,100 | 14,907,597 |