nsv3318982
- Organism: Homo sapiens
- Study:nstd163 (Gupta et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:80
- Publication(s):Gupta et al. 2020
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: 162 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 162 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3318982 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 25,854,105 | 25,854,184 |
| nsv3318982 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 25,834,741 | 25,834,820 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14472002 | Remapped | Perfect | NC_000020.11:g.258 54105_25854184del8 0 | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 25,854,105 | 25,854,184 |
| nssv14472003 | Remapped | Perfect | NC_000020.11:g.258 54105_25854184del8 0 | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 25,854,105 | 25,854,184 |
| nssv14472002 | Submitted genomic | NC_000020.10:g.258 34741_25834820del8 0 | GRCh37 (hg19) | NC_000020.10 | Chr20 | 25,834,741 | 25,834,820 | ||
| nssv14472003 | Submitted genomic | NC_000020.10:g.258 34741_25834820del8 0 | GRCh37 (hg19) | NC_000020.10 | Chr20 | 25,834,741 | 25,834,820 |