nsv6051678
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,014,205
- Publication(s):Wu et al. 2021
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: 3953 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 3954 SVs from 93 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6051678 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000020.11 | Chr20 | 2,825,780 | 3,839,984 | ||
| nsv6051678 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 2,806,426 | 3,820,631 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17620661 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17620661 | Submitted genomic | NC_000020.11:g.282 5780_3839984del | GRCh38 (hg38) | NC_000020.11 | Chr20 | 2,825,780 | 3,839,984 | ||
| nssv17620661 | Remapped | Perfect | NC_000020.10:g.280 6426_3820631del | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 2,806,426 | 3,820,631 |