nsv3070929
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:novel sequence insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:4
- Validation:Not tested
- Clinical Assertions: No
- Data Source:BCMHGSC_JDW
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Variant Region - no placement information
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14042181 | novel sequence insertion | JWB-4147285 | Curated | Curated |
| nssv14043253 | novel sequence insertion | JWB-4053982 | Curated | Curated |
| nssv14041346 | novel sequence insertion | JWB-4057934 | Curated | Curated |
| nssv14039969 | novel sequence insertion | 1104685525271 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv14042181 | Remapped | Good | NT_008046.17:g.571 69751_57202508ins3 2758 | GRCh38.p12 | NT_008046.17 | Chr8|NT_00 8046.17 | 57,169,751 | 57,202,508 |
| nssv14043253 | Remapped | Perfect | NT_010718.17:g.422 344_455101ins32758 | GRCh38.p12 | NT_010718.17 | Chr17|NT_0 10718.17 | 422,344 | 455,101 |
| nssv14041346 | Remapped | Perfect | NT_010783.16:g.396 40893_39673650ins3 2758 | GRCh38.p12 | NT_010783.16 | Chr17|NT_0 10783.16 | 39,640,893 | 39,673,650 |
| nssv14039969 | Remapped | Good | NT_011362.11:g.244 55190_24487731ins3 2758 | GRCh38.p12 | NT_011362.11 | Chr20|NT_0 11362.11 | 24,455,190 | 24,487,731 |