C212082Level 5
t(v;3q26.2)
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A cytogenetic abnormality that refers to a translocation where one of the breakpoints is located in the q26.2 band on the long arm of chromosome 3.
**Synonyms:** - 3q26.2 Translocation - t(3q26.2;v) - t(V;3)(v;q26.2)
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