Genomic Structural Variation

Structured Summary

Abstract

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

MeSH Record

Classification

Broader headings

Genetic Polymorphism

Narrower headings

DNA Copy Number Variations

Related Concepts

Knowledge Graph

Loading graph…

Drag nodes to rearrange; hover to trace links; click a node to open its page.

MeSH Record

Synonyms

23 entry terms

Genome Structural Variants
Genome Structural Variation
Genomic Structural Variants
Genome Structural Variant
Genome Structural Variations
Genomic Structural Variant
Genomic Structural Variations
Structural Variant, Genome
Structural Variant, Genomic
Structural Variants, Genome
Structural Variants, Genomic
Structural Variation, Genome
Structural Variation, Genomic
Structural Variations, Genome
Structural Variations, Genomic
Variant, Genome Structural
Variant, Genomic Structural
Variants, Genome Structural
Variants, Genomic Structural
Variation, Genome Structural
Variation, Genomic Structural
Variations, Genome Structural
Variations, Genomic Structural

MeSH Record

Aspects Covered

5 allowable subheadings

Indexed with the subheadings drug effects, genetics, immunology, physiology, radiation effects.

MeSH Record

History Note

2010

MeSH Hierarchy

Tree Number

G05.365 w.795 w.297w

AMA Style

References

National Library of Medicine. Genomic Structural Variation. Medical Subject Headings (MeSH). 2026. Unique ID D056914. http://id.nlm.nih.gov/mesh/2026/D056914
Genomic Structural Variation. In: Wikipedia. https://en.wikipedia.org/wiki/Structural_variation
Genomic Structural Variation. In: Wikidata. https://www.wikidata.org/wiki/Q7625067