| Accession | HsInv1841 | Region of the inversion | chr8:75245452-75262938 |
| Status | Validated | Prediction type | Simple |
| Estimated Inversion Size | 7,487 bp | Supporting predictions | 1 |
| Inverted allele frequency | ND | Mechanism of origin | ND |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chr8:75245452-75255452 |
| Ancestral orientation | NA | Breakpoint 2 | chr8:75252938-75262938 |
|
|
 |
|
|
Human Polymorphic Inversion DataBase
|
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 | chr8:75250452-75250452 | Breakpoint 2 | chr8:75257938-75257938 |
| Individuals | 54 out of 2504 individuals
 | ||
+ Validation and genotyping
| 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 | Sequence analysis |
| Status | Validated |
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chr8:75245452-75255452 | Breakpoint 2 | chr8:75252938-75262938 | ||
| Definition method | Default informatic definition | ||||
| Mechanism of origin |
ND
|
||||
| Flexibility | 10.19 | GC content | 0.41 | Stability | 1.88 |
+ 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
- 2017-09-18 00:00:00
| Breakpoint 1 | chr8:75245452-75255452 | Breakpoint 2 | chr8:75252938-75262938 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
