Add CNV

[Char-Al]

Currently, SEAL only supports the visualization of SNVs and INDELs. It would be beneficial to expand the functionality of the platform by adding a Copy Number Variation (CNV) view.

CNVs play a crucial role in genetic analysis and can provide valuable insights into genomic variations. By incorporating a CNV view in SEAL, users would have the ability to analyze and interpret CNV data alongside SNVs and INDELs, enabling a more comprehensive understanding of genomic alterations.