nsv6621082
- 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:158,311
- 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: 608 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 608 SVs from 79 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6621082 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 3,227,989 | 3,386,299 |
| nsv6621082 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 3,249,219 | 3,407,529 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18294622 | duplication | OSC4272 | SNP array | Probe signal intensity | nssv18294047, nssv18294943 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18294622 | Remapped | Perfect | NC_000011.10:g.(?_ 3227989)_(3386299_ ?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 3,227,989 | 3,386,299 |
| nssv18294622 | Submitted genomic | NC_000011.9:g.(?_3 249219)_(3407529_? )dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 3,249,219 | 3,407,529 |