nsv4370177
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:62,805
- Publication(s):Zarrei et al. 2019
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: 499 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 499 SVs from 73 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4370177 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 14,497,569 | 14,560,373 |
| nsv4370177 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 14,478,215 | 14,541,019 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15700765 | Remapped | Perfect | NC_000020.11:g.(?_ 14497569)_(1456037 3_?)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 14,497,569 | 14,560,373 |
| nssv15701237 | Remapped | Perfect | NC_000020.11:g.(?_ 14497569)_(1456037 3_?)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 14,497,569 | 14,560,373 |
| nssv15700765 | Submitted genomic | NC_000020.10:g.(?_ 14478215)_(1454101 9_?)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 14,478,215 | 14,541,019 | ||
| nssv15701237 | Submitted genomic | NC_000020.10:g.(?_ 14478215)_(1454101 9_?)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 14,478,215 | 14,541,019 |