DocHub provides a effortless and user-friendly option to copy number in your petition. No matter the intricacies and format of your form, DocHub has all it takes to ensure a quick and headache-free modifying experience. Unlike similar solutions, DocHub stands out for its outstanding robustness and user-friendliness.
DocHub is a web-driven tool allowing you to edit your petition from the comfort of your browser without needing software installations. Owing to its intuitive drag and drop editor, the option to copy number in your petition is quick and straightforward. With rich integration capabilities, DocHub allows you to import, export, and modify paperwork from your selected program. Your updated form will be stored in the cloud so you can access it instantly and keep it safe. You can also download it to your hard drive or share it with others with a few clicks. Alternatively, you can turn your file into a template that stops you from repeating the same edits, including the option to copy number in your petition.
Your edited form will be available in the MY DOCS folder inside your DocHub account. Additionally, you can use our editor panel on the right to combine, split, and convert documents and reorganize pages within your forms.
DocHub simplifies your form workflow by offering an integrated solution!
do you know that over two third of the entire Human Genome comprises of repetitive regions among this about 4 to 10 percent comprises of copy number variations which docHubly contributes to variation in the individuals of our population hello and welcome back to another interesting video of explore bio on genomic series I am Dr Abhishek and in this short video we will learn what a copy number variation is what are the causes of copy number variation how they can be identified and what are their consequences so without any delay lets begin copy number variation or cnv is one of the major causes of a structural variation in the genome in which the number of copies of a particular genome segment gets duplicated or deleted these copy number variations can technically range between thousand bases to 5 megabases but most cnvs are less than 10 KB long in this picture you can see individual 1 has 3 copies of genome segment highlighted in orange color in both the parental chromosomes due