nsv6632126
- 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:213,986
- 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: 637 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 637 SVs from 80 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6632126 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 32,169,802 | 32,383,787 |
| nsv6632126 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 32,209,414 | 32,423,399 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18291172 | duplication | OSC0371 | SNP array | Probe signal intensity | nssv18289600, nssv18289601 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18291172 | Remapped | Perfect | NC_000007.14:g.(?_ 32169802)_(3238378 7_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 32,169,802 | 32,383,787 |
| nssv18291172 | Submitted genomic | NC_000007.13:g.(?_ 32209414)_(3242339 9_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 32,209,414 | 32,423,399 |