| Accession | HsInv0610 | Region of the inversion | chrX:134050426-134253844 |
| Status | Unreliable prediction | Prediction type | Simple |
| Estimated Inversion Size | 132,147 bp | Supporting predictions | 3 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chrX:134050426-134120781 |
| Ancestral orientation | NA | Breakpoint 2 | chrX:134181656-134253844 |
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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:134050426-134095257 | Breakpoint 2 | chrX:134209048-134253844 | ||||||||||||||||||||
| D/C Score | NA | Disc. Support Prob. | 0 | ||||||||||||||||||||
| Support | 3 probes  | ||||||||||||||||||||||
| Individuals |
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| Comments | Below the threshold of the Discordant Support (DS) probability | ||||||||||||||||||||||
| Name | |||||||||||||||||||||||
| Breakpoint 1 | chrX:134109657-134120781 | Breakpoint 2 | chrX:134185401-134193511 | ||||||||||||||||||||
| D/C Score | -4.33 | Disc. Support Prob. | 0 | ||||||||||||||||||||
| Support | 12 probes | ||||||||||||||||||||||
| Individuals |
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| Comments | Below the threshold of the Discordant/Concordant (D/C) ratio score. Below the threshold of the Discordant Support (DS) probability | ||||||||||||||||||||||
| Name | |||||||||||||||||||||||
| Breakpoint 1 | chrX:134082753-134107604 | Breakpoint 2 | chrX:134181656-134206954 | ||||||||||||||||||||
| D/C Score | -1.72 | Disc. Support Prob. | 0 | ||||||||||||||||||||
| Support | 13 probes | ||||||||||||||||||||||
| Individuals |
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| Comments | Below the threshold of the Discordant Support (DS) probability | ||||||||||||||||||||||
+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chrX:134050426-134120781 | Breakpoint 2 | chrX:134181656-134253844 | |||||||||||||
| Description | Breakpoints not refined due to lack of overlap of predictions in at least one breakpoint. Breakpoints calculated without considering unreliable predictions | |||||||||||||||
| Definition method | Default informatic definition | |||||||||||||||
| Mechanism of origin |
ND
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| Flexibility | 10.33 | GC content | 0.35 | Stability | 1.77 |
| Position SD1 | Size (bp) | Position SD2 | Size (bp) | Identity | Relative orientation |
| chrX:134077719-134131328 | 53,610 | chrX:134163328-134225561 | 62,234 | 0.981 | 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
+ Report history
- 2015-02-23 10:14:41
| Breakpoint 1 | chrX:134050426-134120781 | Breakpoint 2 | chrX:134181656-134253844 |
| Assembly | hg18 | ||
| Description | Breakpoints not refined due to lack of overlap of predictions in at least one breakpoint. Breakpoints calculated without considering unreliable predictions | ||
| Definition method | Default informatic definition | ||
- 2015-02-23 10:14:41
| Breakpoint 1 | chrX:134082753-134107604 | Breakpoint 2 | chrX:134185401-134206954 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
