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Genomic structural variation is the variation in structure of an organism's chromosome, such as deletions, duplications, copy-number variants, insertions, inversions and translocations. Originally, a structure variation affects a sequence length about 1kb to 3Mb, which is larger than SNPs and smaller than chromosome abnormality (though the definitions…
Sub-microscopic structural variation, Copy-number variation & Inversion
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structural variation variants genome also duplications deletions methods human genetic inversions sequence insertions chromosome variations cnvs read include however inversion
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Structural variation | is a | variation in structure of an organism's chromosome | 0.90 | text |
| LINEs | instance of | widespread similar sequences | 0.80 | text |
| SINEs may be a common mechanism of CNV creation | instance of | widespread similar sequences | 0.80 | text |
| insertions that escape detection when using other methods | instance of | long read based genome assemblies offer structural variation discovery for classes | 0.80 | text |
| Structural variation | has method | New | 0.60 | section |
| Structural variation | has method | The | 0.60 | section |
| Structural variation | has method | For Genome | 0.60 | section |
| Structural variation | has method | These | 0.60 | section |
| Structural variation | has method | DNA | 0.60 | section |
| Structural variation | has method | This | 0.60 | section |
| Structural variation | has method | For | 0.60 | section |
| Structural variation | has method | PCR | 0.60 | section |
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