nsv5620659
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Ebert et al. 2021
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: 136 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nsv5620659 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 3,531,062 | 3,531,062 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17114176 | insertion | SAMN00006579 | Sequencing | Sequence alignment | 23,265 |
| nssv17114177 | insertion | HG01114 | Sequencing | Sequence alignment | 977 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nssv17114176 | Submitted genomic | NC_000002.12:g.353 1062_3531063ins106 | GRCh38 (hg38) | NC_000002.12 | Chr2 | 3,531,062 | 3,531,062 |
| nssv17114177 | Submitted genomic | NC_000002.12:g.353 1062_3531063ins925 | GRCh38 (hg38) | NC_000002.12 | Chr2 | 3,531,062 | 3,531,062 |