nsv4365651
- 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:59,457
- 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: 194 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 194 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4365651 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 87,899,168 | 87,958,624 |
| nsv4365651 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 87,948,318 | 88,007,774 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15615064 | copy number loss | 1-0139-001 | SNP array | Genotyping | 17 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15615064 | Remapped | Perfect | NC_000003.12:g.(?_ 87899168)_(8795862 4_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 87,899,168 | 87,958,624 |
| nssv15615064 | Submitted genomic | NC_000003.11:g.(?_ 87948318)_(8800777 4_?)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 87,948,318 | 88,007,774 |