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A chromosome mutation is an unpredictable change that occurs in a chromosome. These changes are most often brought on by problems that occur during meiosis (cell division process of gametes) or by mutagens (chemicals, radiation, etc.). chromosome mutation that results in individuals with more than one haploid set of chromosomes in a cell is termed polyploidy. A haploid cell is a cell that contains one complete set of chromosomes.
Mutation is a change in the nucleotide sequence of a gene or a chromosome. Based on the effect of mutation on the gene structure, mutations may be: (1) small-scale mutations or (2) large scale mutations. Small-scale mutations are a type of mutation where one or few nucleotides of a gene are affected. They are further classified as follows: (1) substitution mutations, (2) insertion mutations, and (3) deletion mutations. Insertion mutations are a type of mutation wherein one or more nucleotide base pairs are inserted to a chromosome or a DNA sequence.