nsv5981014
- 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:15,606
- 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: 302 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5981014 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 120,873,039 | 120,888,644 | ||
| nsv5981014 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871056.3 | Chr1|NW_00 3871056.3 | 944,613 | 960,218 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17527189 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17527189 | Submitted genomic | NC_000001.11:g.120 873039_120888644de l | GRCh38 (hg38) | NC_000001.11 | Chr1 | 120,873,039 | 120,888,644 | ||
| nssv17527189 | Remapped | Perfect | NW_003871056.3:g.9 44613_960218del | GRCh37.p13 | First Pass | NW_003871056.3 | Chr1|NW_00 3871056.3 | 944,613 | 960,218 |