A DNA sequence is a CTA - GGA - GCA - T and CTG - GAG - TCG - AT show the result of an insertion mutation in the DNA.
In terms of genomics, insertion is a form of mutation in which one or more nucleotides are inserted into a DNA sequence. Any number of nucleotides can be added during an insertion, ranging from one nucleotide to an entire chromosome (see the below picture).
Insertion refers to the addition of several nucleotides in error to the genome, most frequently while DNA replication is taking place. This quantity can range from one nucleotide to dozens or even millions of them. An insertion's impact differs as well. Others, even single nucleotide insertions, might completely impair a gene's ability to function and result in a pathogenic variant linked to a hereditary disease. Some mutations may have no effect at all.
The four nucleotides that makeup DNA are adenine (A), thymine (T), guanine (G), and cytosine (C) (C). The two DNA strands are connected by base pairs, which are formed when the nucleotides (A with T and G with C) bind to one another. Genes are compact DNA molecules that contain particular genetic information. See the structure of DNA and Nucleotide in below pictures
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