| Accession | HsInv1202 | Region of the inversion | chr10:69002374-69021667 |
| Status | Predicted | Prediction type | Simple |
| Estimated Inversion Size | 9,294 bp | Supporting predictions | 1 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Inverts a region within an intron of a gene | Breakpoint 1 | chr10:69002374-69012374 |
| Ancestral orientation | NA | Breakpoint 2 | chr10:69011667-69021667 |
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Human Polymorphic Inversion DataBase
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General information
- Region map
+ Predictions
| Description | Integrated analysis of structural variants in 2,504 human genomes through short-read and long-read DNA sequencing and statistical imputation using the 1000 Genomes Project data | ||||||||||
| Method | Paired-end mapping (PEM), Long-read sequencing | ||||||||||
| Name | |||
| Breakpoint 1 | chr10:69007374-69007374 | Breakpoint 2 | chr10:69016667-69016667 |
| Individuals | 2 out of 2504 individuals
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+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chr10:69002374-69012374 | Breakpoint 2 | chr10:69011667-69021667 | ||
| Definition method | Default informatic definition | ||||
| Mechanism of origin |
ND
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| Flexibility | 11.97 | GC content | 0.37 | Stability | 1.83 |
+ 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
- CTNNA3
| Gene position | chr10:67349730-69095422 |
| Mechanism | Inverts a region within an intron of a gene |
+ Inversion phenotypical effects
Not defined
+ Report history
- 2017-09-18 00:00:00
| Breakpoint 1 | chr10:69002374-69012374 | Breakpoint 2 | chr10:69011667-69021667 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
