nsv3418770
- 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: 127 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3418770 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 74,346,453 | 74,346,453 | ||
| nsv3418770 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 76,961,369 | 76,961,369 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14782089 | insertion | SAMN04251426 | Sequencing | de novo and local sequence assembly | 22,074 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14782089 | Submitted genomic | NC_000009.12:g.743 46453_74346454ins1 28 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 74,346,453 | 74,346,453 | ||
| nssv14782089 | Remapped | Perfect | NC_000009.11:g.769 61369_76961370ins1 28NC_000009.11:g.7 6961369_76961370in s128 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 76,961,369 | 76,961,369 |