answersLogoWhite

0


Best Answer

Deletion is nothing but eliminating and insertion is adding.

User Avatar

Wiki User

11y ago
This answer is:
User Avatar
More answers
User Avatar

Wiki User

11y ago

Delete erases something. Insert adds something.

This answer is:
User Avatar

Add your answer:

Earn +20 pts
Q: What is the difference betweens deletion and insertion?
Write your answer...
Submit
Still have questions?
magnify glass
imp
Related questions

What do you understand by deque?

A double ended queue (or deque ) is a queue where insertion and deletion can be performed at both end that is front pointer can be used for insertion (apart from its usual operation i.e. deletion) and rear pointer can be used for deletion (apart from its usual operation i.e. insertion)


What are 3 types of mutations and what do they do?

The three different types of mutation are substitution, insertion, and deletion. They differ because deletion is missing a base, insertion has a base that was added, and substitution has a base that has been replaced.


What is a double ended queue?

A double ended queue, or deque, is a queue in which you can access or modify both the head and the tail. The front pointer can be used for insertion (apart from its usual operation i.e. deletion) and rear pointer can be used for deletion (apart from its usual operation i.e. insertion)


What is the need of deque?

A double ended queue (or deque ) is a queue where insertion and deletion can be performed at both end that is front pointer can be used for insertion (apart from its usual operation i.e. deletion) and rear pointer can be used for deletion (apart from its usual operation i.e. insertion). So when we need to insert or delete at both end we need deque.


What is the difference between nucleotide deletion and nucleotide insertion?

Nucleotide deletion removes a nucleotide from a DNA or RNA sequence, resulting in a frameshift mutation that alters the reading frame. Nucleotide insertion adds an extra nucleotide to the sequence, also causing a frameshift mutation. Both types of mutations can have significant impacts on the resulting protein sequence.


Which types of mutation can add genes to a chromosomes?

insertion and deletion


What would produce a frameshift mutation?

An insertion/deletion event.


Difference between circular queue and De queue?

The queue is a linear data structure where operations of insertion and deletion are performed at separate ends also known as front and rear. Queue is a FIFO structure that is first in first out. A circular queue is similar to the normal queue with the difference that queue is circular queue ; that is pointer rear can point to beginning of the queue when it reaches at the end of the queue. Advantage of this type of queue is that empty location let due to deletion of elements using front pointer can again be filled using rear pointer. A double ended queue (or deque ) is a queue where insertion and deletion can be performed at both end that is front pointer can be used for insertion (apart from its usual operation i.e. deletion) and rear pointer can be used for deletion (apart from its usual operation i.e. insertion)


Is spina bifida insertion or deletion issue?

As far as we know, spina bifida doesn't have a specific chromosomal abnormality, so it isn't thought of as an insertion or deletion. It is a developmental problem with the neural tube.


What do insertion and deletion have in common?

Both of them affect the length.


What are 3 types of mutation?

The three types of mutations are substitution (where one base is replaced with another), insertion (where an extra base is added), and deletion (where a base is removed). These mutations can alter the DNA sequence and potentially change the resulting protein.


Which is not a frameshift mutation substitution insertion deletion or point mutation?

A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.