nsv3167791
- Organism: Homo sapiens
- Study:nstd158 (Cleal et al. 2019)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:185,676,834
- Publication(s):Cleal 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: 391637 SVs from 160 studies. See in: genome view
Overlapping variant regions from other studies: 390067 SVs from 160 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3167791 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 41,948,882 (-487, +487) | 227,625,715 (-487, +487) |
| nsv3167791 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 42,414,553 (-487, +487) | 227,813,416 (-487, +487) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14239776 | inversion | DB116 | Sequencing | Paired-end mapping | 36 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14239776 | Remapped | Good | NC_000001.11:g.(41 948395_41949369)_( 227625228_22762620 2)inv | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 41,948,882 (-487, +487) | 227,625,715 (-487, +487) |
| nssv14239776 | Submitted genomic | NC_000001.10:g.(42 414066_42415040)_( 227812929_22781390 3)inv | GRCh37 (hg19) | NC_000001.10 | Chr1 | 42,414,553 (-487, +487) | 227,813,416 (-487, +487) |