nsv3168805
- 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:67,052,259
- 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: 194687 SVs from 151 studies. See in: genome view
Overlapping variant regions from other studies: 194361 SVs from 151 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3168805 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 12,297,088 (-331, +331) | 79,349,346 (-331, +331) |
| nsv3168805 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 12,297,321 (-331, +331) | 80,059,063 (-331, +331) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14239866 | inversion | DB51 | Sequencing | Paired-end mapping | 89 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14239866 | Remapped | Good | NC_000006.12:g.(12 296757_12297419)_( 79349015_79349677) inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 12,297,088 (-331, +331) | 79,349,346 (-331, +331) |
| nssv14239866 | Submitted genomic | NC_000006.11:g.(12 296990_12297652)_( 80058732_80059394) inv | GRCh37 (hg19) | NC_000006.11 | Chr6 | 12,297,321 (-331, +331) | 80,059,063 (-331, +331) |