esv3755086
- 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:381,939
- Description:Chr3:g.2406580_2788518inv
- Publication(s):Berger 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: 1778 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 1778 SVs from 94 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3755086 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 2,364,896 | 2,746,834 |
| esv3755086 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 2,406,580 | 2,788,518 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16578064 | inversion | 1669609 | Curated | Curated | 80 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16578064 | Remapped | Perfect | NC_000003.12:g.236 4896_2746834inv | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 2,364,896 | 2,746,834 |
| essv16578064 | Submitted genomic | NC_000003.11:g.240 6580_2788518inv | GRCh37 (hg19) | NC_000003.11 | Chr3 | 2,406,580 | 2,788,518 |