a. Novelty based on overlap of our SV set with DGV19 (upper panel i, broken down by SV class), of collapsed CNVRs with earlier 1000 Genomes Project releases6,8 (ii) and of our SV set with refs6,8 (iii). b. Size distribution of ascertained SVs (bin width is uniform in log-scale). DEL, biallelic deletion, DUP, biallelic duplication, INV, inversion, INS, non-reference insertion (including MEIs and NUMTs). c. Breakpoint precision of assembled deletions stratified by VAF (split-read caller Pindel23 shown separately). d. SV allele sharing across continental groups. f. LD properties of biallelic SV classes.