nsv5914382
- 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:9,534,083
- 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: 26714 SVs from 127 studies. See in: genome view
Overlapping variant regions from other studies: 26714 SVs from 127 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5914382 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 27,312,316 | 36,846,398 | ||
| nsv5914382 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 27,601,245 | 37,135,326 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17355429 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17355429 | Submitted genomic | NC_000010.11:g.273 12316_36846398del | GRCh38 (hg38) | NC_000010.11 | Chr10 | 27,312,316 | 36,846,398 | ||
| nssv17355429 | Remapped | Perfect | NC_000010.10:g.276 01245_37135326del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 27,601,245 | 37,135,326 |