nsv5887334
- 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:1,602,457
- 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: 3409 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 3405 SVs from 84 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5887334 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 119,471,365 | 121,073,821 | ||
| nsv5887334 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 118,605,328 | 120,207,675 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17437370 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17437370 | Submitted genomic | NC_000023.11:g.119 471365_121073821de l | GRCh38 (hg38) | NC_000023.11 | ChrX | 119,471,365 | 121,073,821 | ||
| nssv17437370 | Remapped | Good | NC_000023.10:g.118 605328_120207675de l | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 118,605,328 | 120,207,675 |