nsv1154282
- Organism: Homo sapiens
- Study:nstd105 (Onozawa et al. 2015)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:312
- Description:Insertion of chr3:16406447-16410413
- Publication(s):Onozawa et al. 2015
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: 375 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 376 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154282 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 7,720,378 | 7,720,689 |
| nsv1154282 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 7,588,419 | 7,588,730 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004120 | Remapped | Perfect | NC_000024.10:g.(77 20378_?)_(?_772068 9)ins3966 | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 7,720,378 | 7,720,689 |
| nssv4004120 | Submitted genomic | NC_000024.9:g.(758 8419_?)_(?_7588730 )ins3966 | GRCh37 (hg19) | NC_000024.9 | ChrY | 7,588,419 | 7,588,730 |