esv3787012
- 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:292,299
- Description:Chr8:g.108236482_108528780inv
- 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: 985 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 985 SVs from 76 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3787012 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 107,224,254 | 107,516,552 |
| esv3787012 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 108,236,482 | 108,528,780 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16613627 | inversion | 1673902 | Curated | Curated | 60 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16613627 | Remapped | Perfect | NC_000008.11:g.107 224254_107516552in v | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 107,224,254 | 107,516,552 |
| essv16613627 | Submitted genomic | NC_000008.10:g.108 236482_108528780in v | GRCh37 (hg19) | NC_000008.10 | Chr8 | 108,236,482 | 108,528,780 |