| Accession | HsInv0078 | Region of the inversion | chrX:53868477-53870595 |
| Status | Predicted | Prediction type | Simple |
| Estimated Inversion Size | 1,835 bp | Supporting predictions | 1 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chrX:53868477-53868762 |
| Ancestral orientation | NA | Breakpoint 2 | chrX:53870313-53870595 |
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Human Polymorphic Inversion DataBase
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General information
- Region map
+ Predictions
| Description | Sequencing and analysis of the independently assembled diploid J. Craig Venter genome (HuRef) | ||||||||||||||
| Method | Genome sequence comparison | ||||||||||||||
| Name | |||||||
| Breakpoint 1 | chrX:53868900-53868900 | Breakpoint 2 | chrX:53870123-53870123 | ||||
| Individuals |
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+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chrX:53868477-53868762 | Breakpoint 2 | chrX:53870313-53870595 | ||
| Description | Breakpoints defined by comparison with HuRef Human Genome assembly | ||||
| Definition method | Manual curation | ||||
| Mechanism of origin |
ND
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| Flexibility | 10.95 | GC content | 0.56 | Stability | 2.07 |
+ 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 10:15:26
| Breakpoint 1 | chrX:53867900-53869900 | Breakpoint 2 | chrX:53869123-53871123 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
- 2015-02-23 10:15:26
| Breakpoint 1 | chrX:53868477-53868762 | Breakpoint 2 | chrX:53870313-53870595 |
| Assembly | hg18 | ||
| Description | Breakpoints defined by comparison with HuRef Human Genome assembly | ||
| Definition method | Manual curation | ||
