nsv5929452
- 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:7,550,334
- 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: 23105 SVs from 131 studies. See in: genome view
Overlapping variant regions from other studies: 23106 SVs from 131 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5929452 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 6,412,133 | 13,962,466 | ||
| nsv5929452 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 6,315,453 | 13,865,783 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17377901 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17377901 | Submitted genomic | NC_000017.11:g.641 2133_13962466del | GRCh38 (hg38) | NC_000017.11 | Chr17 | 6,412,133 | 13,962,466 | ||
| nssv17377901 | Remapped | Perfect | NC_000017.10:g.631 5453_13865783del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 6,315,453 | 13,865,783 |