This form allows you to quickly access the CADD-SV scores and corresponding annotation for all pre-scored SVs. This currently includes gnomAD structural variant release v2.1, structural variants from ClinVar, the 1000 Genomes project as well as from Abel HJ et al. 2020 and Beyter D et al. 2021. Please note that all variants were originally scored on GRCh38 and that coordinates are provided as such. However, we allow to specifiy coordinates on NCBI36/hg18 or GRCh37/hg19 for variant retrieval, which are converted using liftOver.