esv3782058
- 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:79,951
- Description:Chr11:g.78804985_78884935inv
- Publication(s):Berger et al. 2012, Forbes et al. 2008, Forbes et al. 2008
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: 273 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 273 SVs from 50 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3782058 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 79,093,940 | 79,173,890 |
| esv3782058 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 78,804,985 | 78,884,935 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16608127 | inversion | 1673896 | Curated | Curated | 182 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16608127 | Remapped | Perfect | NC_000011.10:g.790 93940_79173890inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 79,093,940 | 79,173,890 |
| essv16608127 | Submitted genomic | NC_000011.9:g.7880 4985_78884935inv | GRCh37 (hg19) | NC_000011.9 | Chr11 | 78,804,985 | 78,884,935 |