Spinner


as

feature_translocation    (CURRENT_SVN)

SO Accession: SO:0001881 (SOWiki)
Definition: A sequence variant, caused by an alteration of the genomic sequence, where the structural change, a translocation, is greater than the extent of the underlying genomic features.
Synonyms: feature translocation
DB Xrefs: SO: ke

Parent: structural_variant (SO:0001537)

Children: regulatory_region_translocation (SO:0001884)
transcript_translocation (SO:0001883)
In the image below graph nodes link to the appropriate terms. Clicking the image background will toggle the image between large and small formats.
Graph image for SO:0001881