nsv5956621
- 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:2,015,531
- 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: 9935 SVs from 133 studies. See in: genome view
Overlapping variant regions from other studies: 10887 SVs from 137 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5956621 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000022.11 | Chr22 | 22,621,614 | 24,637,144 | ||
| nsv5956621 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000022.10 | Chr22 | 22,964,084 | 25,033,111 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17405775 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17405775 | Submitted genomic | NC_000022.11:g.226 21614_24637144del | GRCh38 (hg38) | NC_000022.11 | Chr22 | 22,621,614 | 24,637,144 | ||
| nssv17405775 | Remapped | Good | NC_000022.10:g.229 64084_25033111del | GRCh37.p13 | First Pass | NC_000022.10 | Chr22 | 22,964,084 | 25,033,111 |