| Accession | HsInv1042 | Region of the inversion | chr2:116694167-116699135 |
| Status | Obsolete | Prediction type | Simple |
| Estimated Inversion Size | 4,035 bp | Supporting predictions | 1 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chr2:116694167-116695112 |
| Ancestral orientation | NA | Breakpoint 2 | chr2:116698213-116699135 |
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Human Polymorphic Inversion DataBase
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General information
- Region map
+ Predictions
| Description | Next generation sequencing and analysis by paired-end mapping of a Korean individual genome | ||||||||||||||
| Method | Paired-end mapping (PEM) | ||||||||||||||
| Name | |||||||
| Breakpoint 1 | chr2:116694512-116694767 | Breakpoint 2 | chr2:116698535-116698813 | ||||
| Individuals |
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+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chr2:116694167-116695112 | Breakpoint 2 | chr2:116698213-116699135 | ||
| Definition method | Default informatic definition | ||||
| Mechanism of origin |
ND
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| Flexibility | 11.04 | GC content | 0.43 | Stability | 1.87 |
+ Evolutionary history
| Ancestral allele | NA | Age | ND |
| Derived allele | NA | Origin | ND |
+ Orientation in other species
Not defined
+ Age
Not defined
+ Origin
Not defined
+ Functional effects
No genes disrupted by the inversion breakpoints
+ Inversion phenotypical effects
Not defined
