t(7;16)(q33;p11)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A cytogenetic abnormality that refers to a chromosomal translocation involving the long arm (q33) of chromosome 7 and the short arm (p11) of chromosome 16. It is associated with the expression of FUS/CREB3L2 fusions and is a characteristic feature of low grade fibromyxoid sarcoma.