nsv6633489
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:34,364
- Publication(s):Zarrei et al. 2023
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: 250 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 250 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6633489 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 85,156,927 | 85,191,290 |
| nsv6633489 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 87,771,842 | 87,806,205 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18282629 | deletion | OSC0216 | SNP array | Probe signal intensity | nssv18282010, nssv18282622, nssv18282625 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18282629 | Remapped | Perfect | NC_000009.12:g.(?_ 85156927)_(8519129 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 85,156,927 | 85,191,290 |
| nssv18282629 | Submitted genomic | NC_000009.11:g.(?_ 87771842)_(8780620 5_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 87,771,842 | 87,806,205 |