| Accession | HsInv0052 | Region of the inversion | chr3:164027658-164030968 |
| Status | Obsolete | Prediction type | Simple |
| Estimated Inversion Size | 2,333 bp | Supporting predictions | 2 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chr3:164027658-164028657 |
| Ancestral orientation | NA | Breakpoint 2 | chr3:164030012-164030968 |
| Comments | Inversion corresponds to a multiallelic variant according to Pang et al. 2012
|
||
|
|
 |
|
|
Human Polymorphic Inversion DataBase
|
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 | chr3:164028057-164028258 | Breakpoint 2 | chr3:164030368-164030612 | ||||
| Individuals |
| ||||||
| Description | Sequencing and analysis of the independently assembled diploid J. Craig Venter genome (HuRef) | ||||||||||||||
| Method | Genome sequence comparison | ||||||||||||||
| Name | |||||||
| Breakpoint 1 | chr3:164028056-164028056 | Breakpoint 2 | chr3:164030335-164030335 | ||||
| Individuals |
| ||||||
+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chr3:164027658-164028657 | Breakpoint 2 | chr3:164030012-164030968 | ||
| Definition method | Default informatic definition | ||||
| Mechanism of origin |
ND
|
||||
| Flexibility | 10.55 | GC content | 0.32 | Stability | 1.79 |
+ 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
