nsv6621279
- 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:347,958
- 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: 1479 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1479 SVs from 88 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6621279 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 89,687,439 | 90,035,396 |
| nsv6621279 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 89,420,607 | 89,768,564 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18292533 | duplication | OSC3882 | SNP array | Probe signal intensity | 8 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18292533 | Remapped | Perfect | NC_000011.10:g.(?_ 89687439)_(9003539 6_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 89,687,439 | 90,035,396 |
| nssv18292533 | Submitted genomic | NC_000011.9:g.(?_8 9420607)_(89768564 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 89,420,607 | 89,768,564 |