insertion/deletion variant

Aliases

indel, insertions/deletions

External links

ClinVar

No related entities found.

Mentioned in (8)

Papers in which this entity is mentioned.

• ConsensuSV-ONT - A modern method for accurate structural variant calling. (2025)
• The Application of Long-Read Sequencing to Cancer. (2024)
• Detection of somatic structural variants from short-read next-generation sequencing data. (2021)
• Multi-cancer analysis of clonality and the timing of systemic spread in paired primary tumors and metastases. (2020)
• Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
• HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
• The impact of structural variation on human gene expression. (2017)
• VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)

Merged raw entities (2)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.