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| Term | chromosomal_inversion | ID (Ontology) | SO:1000030 (Sequence Ontology) | |||||
| Definition | An interchromosomal mutation where a region of the chromosome is inverted with respect to wild type. | |||||||
| Also Known As | "chromosomal inversion" | |||||||
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| SO.org | ||||||||
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| Records annotated with this term OR any of its CHILD TERMS | ||||||||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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chromosome_structure_variation |__intrachromosomal_mutation |__chromosomal_inversion 4487 rec. |__bipartite_inversion 48 rec. |__deficient_inversion 81 rec. |__inversion_cum_translocation 234 rec. | |__inverted_intrachromosomal_transposition 42 rec. |__inverted_ring_chromosome 1 rec. |__paracentric_inversion 4 rec. |__pericentric_inversion |
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| Is a | intrachromosomal_mutation | ||
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External Crossreferences & Linkouts
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| http://en.wikipedia.org/wiki/Chromosomal_inversion "wiki" | |||