| Accession | HsInv0391 | Region of the inversion | chrX:51422445-51493352 |
| Status | Obsolete | Prediction type | Simple |
| Estimated Inversion Size | 44,036 bp | Supporting predictions | 1 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chrX:51422445-51446040 |
| Ancestral orientation | NA | Breakpoint 2 | chrX:51463204-51493352 |
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Human Polymorphic Inversion DataBase
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General information
- Region map
+ Predictions
- Martinez-Fundichely et al. 2014 (in preparation)
| Description | Accurate prediction of inversions in the human genome from Kidd et al. 2008 fosmid paired-end mapping data using the GRIAL algorithm, and validation of some predictions by sequence analysis and PCR | ||||||||||||||||||||||||||||||||||||||
| Method | Paired-end mapping (PEM) | ||||||||||||||||||||||||||||||||||||||
| Name | |||||||||||||||||||||||
| Breakpoint 1 | chrX:51422445-51446040 | Breakpoint 2 | chrX:51463204-51493352 | ||||||||||||||||||||
| D/C Score | -0.41 | Disc. Support Prob. | 0.97227 | ||||||||||||||||||||
| Support | 28 probes  | ||||||||||||||||||||||
| Individuals |
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+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chrX:51422445-51446040 | Breakpoint 2 | chrX:51463204-51493352 | |||||||||||||
| Definition method | Default informatic definition | |||||||||||||||
| Mechanism of origin |
ND
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| Flexibility | 10.91 | GC content | 0.4 | Stability | 1.84 |
| Position SD1 | Size (bp) | Position SD2 | Size (bp) | Identity | Relative orientation |
| chrX:51426997-51452741 | 25,745 | chrX:51460141-51485500 | 25,360 | 0.997 | Inverted |
+ 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
