nsv3418796
- Organism: Homo sapiens
- Study:nstd162 (Audano et al. 2019)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Audano et al. 2019
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: 236 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 37 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3418796 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 134,760,350 | 134,760,350 | ||
| nsv3418796 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 137,652,196 | 137,652,196 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14775899 | insertion | SAMN06885952 | Sequencing | de novo and local sequence assembly | 28,070 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14775899 | Submitted genomic | NC_000009.12:g.134 760350_134760351in s76 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 134,760,350 | 134,760,350 | ||
| nssv14775899 | Remapped | Perfect | NC_000009.11:g.137 652196_137652197in s76NC_000009.11:g. 137652196_13765219 7ins76 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 137,652,196 | 137,652,196 |