chromosome_structure_variation (CURRENT_RELEASE) |
|
|---|---|
| SO Accession: | SO:1000183 (SOWiki) |
| Definition: | An alteration of the genome that leads to a change in the structure or number of one or more chromosomes. |
| Synonyms: | chromosome structure variation, snpEff:CHROMOSOME_LARGE_DELETION |
| Parent: | chromosome_variation (SO:0000240) |
| Children: | autosynaptic_chromosome (SO:1000136) |
| aneuploid_chromosome (SO:0000550) | |
| compound_chromosome (SO:1000042) | |
| intrachromosomal_mutation (SO:1000028) | |
| chromosomal_duplication (SO:1000037) | |
| chromosomal_transposition (SO:0000453) | |
| complex_structural_alteration (SO:0001784) | |
| free_chromosome_arm (SO:0000065) | |
| uncharacterized_chromosomal_mutation (SO:1000170) | |
| interchromosomal_mutation (SO:1000031) | |
In the image below graph nodes link to the appropriate terms. Clicking the image background will toggle the image between large and small formats.
