nsv6633713
- 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:59,646
- 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: 503 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 509 SVs from 59 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6633713 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 21,157,374 | 21,217,019 |
| nsv6633713 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 21,157,373 | 21,217,018 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18287978 | duplication | OSC0336 | SNP array | Probe signal intensity | 5 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18287978 | Remapped | Perfect | NC_000009.12:g.(?_ 21157374)_(2121701 9_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 21,157,374 | 21,217,019 |
| nssv18287978 | Submitted genomic | NC_000009.11:g.(?_ 21157373)_(2121701 8_?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 21,157,373 | 21,217,018 |