nsv5981658
- 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:290,124
- 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: 907 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 911 SVs from 83 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5981658 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 162,104,471 | 162,394,594 | ||
| nsv5981658 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 162,074,261 | 162,364,384 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17522472 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17522472 | Submitted genomic | NC_000001.11:g.162 104471_162394594du p | GRCh38 (hg38) | NC_000001.11 | Chr1 | 162,104,471 | 162,394,594 | ||
| nssv17522472 | Remapped | Perfect | NC_000001.10:g.162 074261_162364384du p | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 162,074,261 | 162,364,384 |