esv3791957
- 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:83,521
- Description:Chr7:g.52377218_52460738inv
- 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: 326 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 326 SVs from 53 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3791957 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 52,309,522 | 52,393,042 |
| esv3791957 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 52,377,218 | 52,460,738 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16619181 | inversion | 1673902 | Curated | Curated | 60 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16619181 | Remapped | Perfect | NC_000007.14:g.523 09522_52393042inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 52,309,522 | 52,393,042 |
| essv16619181 | Submitted genomic | NC_000007.13:g.523 77218_52460738inv | GRCh37 (hg19) | NC_000007.13 | Chr7 | 52,377,218 | 52,460,738 |