genomic structural variation

Preferred Label : genomic structural variation;

MeSH definition : Contiguous large-scale (1000-400,000 basepairs) differences in the genomic DNA between individuals, due to SEQUENCE DELETION; SEQUENCE INSERTION; or SEQUENCE INVERSION.;

MeSH synonym : genome structural variant; genome structural variations; genomic structural variants; genomic structural variations; structural variant, genomic; structural variants, genome; structural variation, genomic; structural variations, genome; variants, genomic structural; variations, genomic structural; structural variant, genome; variant, genome structural; variants, genome structural; structural variations, genomic; variation, genomic structural; genome structural variation; structural variation, genome; variation, genome structural; variations, genome structural; genomic structural variant; structural variants, genomic; variant, genomic structural; genome structural variants;

Details

Origin ID

D056914;

UMLS CUI

C2717924;

Allowable qualifiers
- drug effects [MeSH Qualifier]
- genetics [MeSH Qualifier]
- immunology [MeSH Qualifier]
- physiology [MeSH Qualifier]
- radiation effects [MeSH Qualifier]
CISMeF manual mappings
- Structural variation [OMIConto structure]
Currated CISMeF NLP mapping
- Structural variation [EDAM topic]
Record concept(s)
- genomic structural variation [MeSH concept]
See also inter- (CISMeF)
- Structural variation databases [OMIConto index]
- Structural variation identification (DNA-seq analysis) [OMIConto index]
Semantic type(s)
- Genetic Function [UMLS semantic type]
UMLS correspondences (same concept)
- Structural variation [EDAM topic]
- Structural variation [OMIConto structure]

Keyword's position in hierarchy(ies) :

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