nsv5990783
- 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:1,820,132
- 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: 5455 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 5449 SVs from 102 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5990783 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 10,050,341 | 11,870,472 | ||
| nsv5990783 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 10,092,025 | 11,911,946 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17531828 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17531828 | Submitted genomic | NC_000003.12:g.100 50341_11870472del | GRCh38 (hg38) | NC_000003.12 | Chr3 | 10,050,341 | 11,870,472 | ||
| nssv17531828 | Remapped | Good | NC_000003.11:g.100 92025_11911946del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 10,092,025 | 11,911,946 |