nsv6626063
- 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:41,906
- 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: 353 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 353 SVs from 51 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6626063 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 189,867,559 | 189,909,464 |
| nsv6626063 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 189,836,689 | 189,878,594 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18297526 | deletion | OSC4814 | SNP array | Probe signal intensity | nssv18297194, nssv18296632 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18297526 | Remapped | Perfect | NC_000001.11:g.(?_ 189867559)_(189909 464_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,867,559 | 189,909,464 |
| nssv18297526 | Submitted genomic | NC_000001.10:g.(?_ 189836689)_(189878 594_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 189,836,689 | 189,878,594 |