esv3755377
- 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:71,908
- Description:Chr4:g.92087643_92159550inv
- Publication(s):Bass et al. 2011, 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: 294 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 294 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3755377 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 91,166,492 | 91,238,399 |
| esv3755377 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 92,087,643 | 92,159,550 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16578385 | inversion | 1565440 | Curated | Curated | 180 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16578385 | Remapped | Perfect | NC_000004.12:g.911 66492_91238399inv | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 91,166,492 | 91,238,399 |
| essv16578385 | Submitted genomic | NC_000004.11:g.920 87643_92159550inv | GRCh37 (hg19) | NC_000004.11 | Chr4 | 92,087,643 | 92,159,550 |