nsv5933606
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:8,855,519
- Publication(s):Almarri 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: 23713 SVs from 135 studies. See in: genome view
Overlapping variant regions from other studies: 23716 SVs from 135 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5933606 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000015.10 | Chr15 | 71,577,714 | 80,433,232 | ||
| nsv5933606 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 71,870,053 | 80,725,573 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17387138 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17387138 | Submitted genomic | NC_000015.10:g.715 77714_80433232del | GRCh38 (hg38) | NC_000015.10 | Chr15 | 71,577,714 | 80,433,232 | ||
| nssv17387138 | Remapped | Perfect | NC_000015.9:g.7187 0053_80725573del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 71,870,053 | 80,725,573 |