nsv4381661
- 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:166,250
- 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: 1067 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 709 SVs from 77 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4381661 | Remapped | Pass | GRCh38.p12 | Primary Assembly | Second Pass | NC_000009.12 | Chr9 | 40,937,364 | 41,103,613 |
| nsv4381661 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 68,671,563 | 69,002,883 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15613717 | copy number loss | 1-0718-003 | SNP array | Genotyping | 35 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15613717 | Remapped | Pass | NC_000009.12:g.(?_ 40937364)_(4110361 3_?)del | GRCh38.p12 | Second Pass | NC_000009.12 | Chr9 | 40,937,364 | 41,103,613 |
| nssv15613717 | Submitted genomic | NC_000009.11:g.(?_ 68671563)_(6900288 3_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 68,671,563 | 69,002,883 |