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Annotate a single structural variant with StrVCTVRE

You may use this form to score a structural variant with StrVCTVRE. The variant must be at least 50 bp in length. Please use capital letters for sex chromosomes (e.g. X or chrX).
Select variant type
Select genome build
By clicking 'Annotate variant', you confirm that you have the authority to provide this information to StrVCTVRE. Your variant will be immediately deleted from our server. You hereby irrevocably agree to hold the StrVCTVRE developers harmless from any form of liability if the data that you provide becomes compromised.
Please click 'Annotate variant' only once. After several seconds you will be redirected to a page that displays the StrVCTVRE score of your variant.
If you use StrVCTVRE in your published work, please cite:
Sharo AG, Hu Z, Sunyaev SR, and Brenner SE. 2022. StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants. The American Journal of Human Genetics 109:195-209. doi:10.1016/j.ajhg.2021.12.007