esv3763083
- 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:85,987
- Description:Chr20:g.6104872_6190858inv
- 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: 356 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 356 SVs from 60 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3763083 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 6,124,225 | 6,210,211 |
| esv3763083 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 6,104,872 | 6,190,858 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16587015 | inversion | 1737653 | Curated | Curated | 19 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16587015 | Remapped | Perfect | NC_000020.11:g.612 4225_6210211inv | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 6,124,225 | 6,210,211 |
| essv16587015 | Submitted genomic | NC_000020.10:g.610 4872_6190858inv | GRCh37 (hg19) | NC_000020.10 | Chr20 | 6,104,872 | 6,190,858 |