| Accession | HsInv1851 | Region of the inversion | chr11:70946755-70957083 |
| Status | Predicted | Prediction type | Simple |
| Estimated Inversion Size | 329 bp | Supporting predictions | 1 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chr11:70946755-70956755 |
| Ancestral orientation | NA | Breakpoint 2 | chr11:70947083-70957083 |
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Human Polymorphic Inversion DataBase
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General information
- Region map
+ Predictions
| Description | Identification and resolution of sequence gaps and structural variants in the euchromatic regions of the reference human assembly through single-molecule, real-time (SMRT) DNA sequencing of an haploid human genome (CHM1) | ||||||||||||||
| Method | Long-read sequencing | ||||||||||||||
| Name | |||||||
| Breakpoint 1 | chr11:70951755-70951755 | Breakpoint 2 | chr11:70952083-70952083 | ||||
| Individuals |
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+ Validation and genotyping
No validations are found
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chr11:70946755-70956755 | Breakpoint 2 | chr11:70947083-70957083 | ||
| Definition method | Default informatic definition | ||||
| Mechanism of origin |
ND
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| Flexibility | 10.97 | GC content | 0.35 | Stability | 1.77 |
+ 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
- 2017-09-29 00:00:00
| Breakpoint 1 | chr11:70946755-70956755 | Breakpoint 2 | chr11:70947083-70957083 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
