nsv6631792
- 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:88,969
- 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: 826 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 822 SVs from 61 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6631792 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 94,834,615 | 94,923,583 |
| nsv6631792 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 95,544,333 | 95,633,301 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18285993 | deletion | OSC2729 | SNP array | Probe signal intensity | nssv18285400, nssv18286314, nssv18285992 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18285993 | Remapped | Perfect | NC_000006.12:g.(?_ 94834615)_(9492358 3_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 94,834,615 | 94,923,583 |
| nssv18285993 | Submitted genomic | NC_000006.11:g.(?_ 95544333)_(9563330 1_?)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 95,544,333 | 95,633,301 |