nsv4366962
- 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:72,542
- 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: 2583 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 2583 SVs from 97 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4366962 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 78,259,375 | 78,331,916 |
| nsv4366962 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 78,969,092 | 79,041,633 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15656700 | Remapped | Perfect | NC_000006.12:g.(?_ 78259375)_(7833191 6_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 78,259,375 | 78,331,916 |
| nssv15689247 | Remapped | Perfect | NC_000006.12:g.(?_ 78259375)_(7833191 6_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 78,259,375 | 78,331,916 |
| nssv15656700 | Submitted genomic | NC_000006.11:g.(?_ 78969092)_(7904163 3_?)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 78,969,092 | 79,041,633 | ||
| nssv15689247 | Submitted genomic | NC_000006.11:g.(?_ 78969092)_(7904163 3_?)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 78,969,092 | 79,041,633 |