Detected Variant Classes

The SV Caller can discover all variation classes that can be explained as novel DNA adjacencies in the genome. Novel DNA adjacencies are classified into the following categories based on the breakend pattern:

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Deletions

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Insertions. SV insertions can be divided into the following two subclasses depending on if the inserted sequence can be fully assembled.

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Fully-assembled insertions

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Partially-assembled (ie. inferred) insertions

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Tandem Duplications

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Unclassified breakend pairs corresponding to intra- and inter-chromosomal translocations, or complex structural variants.