delins [SO_1000032]
delins
ID: SO_1000032
A sequence alteration which included an insertion and a deletion, affecting 2 or more bases.
Indels can have a different number of bases than the corresponding reference sequence. The term name was changed from indel to delins on 2/24/2019 to align with the HGVS nomenclature term for a deletion-insertion. Indel was causing confusion in the annotation community (github issue 445). The HGVS nomenclature definition of deletion-insertion (delins) is a sequence change where, compared to a reference sequence, one or more nucleotides are replaced by one or more other nucleotides and which is not a substitution, inversion or conversion.Indels can have a different number of bases than the corresponding reference sequence.
Open in VFB 3D Browser →Classification
Alternative Names
| Synonym | Scope | Reference |
|---|---|---|
| deletion-insertion | exact synonym | |
| indel | exact synonym |
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