| Accession | HsInv0589 | Region of the inversion | chr7:150640767-150643414 |
| Status | False | Prediction type | Simple |
| Estimated Inversion Size | 1,864 bp | Supporting predictions | 3 |
| Inverted allele frequency | NA | Mechanism of origin | NA |
| Functional effect | Intergenic breakpoints | Breakpoint 1 | chr7:150640767-150641573 |
| Ancestral orientation | NA | Breakpoint 2 | chr7:150642652-150643414 |
| Comments | False inversion prediction caused by an inverted duplication
|
||
|
|
 |
|
|
Human Polymorphic Inversion DataBase
|
General information
- Region map
+ Predictions
| Description | Discovery, genotyping and phasing of structural variants detected from Illumina whole genome sequencing data of 769 individuals from 250 Dutch families belonging to the GoNL project | ||||||||||
| Method | Paired-end mapping (PEM) | ||||||||||
| Name | |||
| Breakpoint 1 | chr7:150641350-150641350 | Breakpoint 2 | chr7:150642978-150642978 |
| Individuals | |||
| 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 | chr7:150640963-150640963 | Breakpoint 2 | chr7:150643040-150643040 |
| Individuals | 1080 out of 2504 individuals
 | ||
| Description | Next generation sequencing and analysis by paired-end mapping of a Korean individual genome | ||||||||||||||
| Method | Paired-end mapping (PEM) | ||||||||||||||
| Name | |||||||
| Breakpoint 1 | chr7:150640973-150641367 | Breakpoint 2 | chr7:150642814-150643252 | ||||
| Individuals |
| ||||||
+ Validation and genotyping
| Description | Discovery, genotyping and phasing of structural variants detected from Illumina whole genome sequencing data of 769 individuals from 250 Dutch families belonging to the GoNL project | ||||
| Method | Polymerase chain reaction (PCR) |
| Status | Validated |
| Comment | Tested in sample A105c |
| 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 | False |
| Comment | Inverted duplication validated by sequence analysis of PacBio long reads from long-range PCR amplicons, PacBio long reads from fosmids |
+ Frequency
No frequency studied
+ Breakpoints
| Breakpoint 1 | chr7:150640767-150641573 | Breakpoint 2 | chr7:150642652-150643414 | ||
| Definition method | Default informatic definition | ||||
| Mechanism of origin |
NA
|
||||
| Flexibility | 11.01 | GC content | 0.4 | Stability | 1.72 |
+ 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 | chr7:150640767-150641573 | Breakpoint 2 | chr7:150642652-150643414 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
- 2017-09-18 00:00:00
| Breakpoint 1 | chr7:150640767-150641573 | Breakpoint 2 | chr7:150642652-150643414 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
- 2015-02-23 10:15:10
| Breakpoint 1 | chr7:150640767-150641573 | Breakpoint 2 | chr7:150642652-150643414 |
| Assembly | hg18 | ||
| Definition method | Default informatic definition | ||
