esv3755246
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:inversion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:586,509
- Description:Chr4:g.134382847_134969355inv
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Fujimoto et al. 2012
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: 1534 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1534 SVs from 84 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3755246 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 133,461,692 | 134,048,200 |
| esv3755246 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 134,382,847 | 134,969,355 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16578236 | inversion | 1737642 | Curated | Curated | essv16602079 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16578236 | Remapped | Perfect | NC_000004.12:g.133 461692_134048200in v | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 133,461,692 | 134,048,200 |
| essv16578236 | Submitted genomic | NC_000004.11:g.134 382847_134969355in v | GRCh37 (hg19) | NC_000004.11 | Chr4 | 134,382,847 | 134,969,355 |