A new data collection and preprint describing structural variants from 1,019 samples from twenty-six 1000 Genomes Project populations is available.
Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project by Schloissnig,et al uses intermediate-level long read sequencing and a novel method integrating linear and graph based calling methods to type over 160,000 structural variants in this population scale catalogue.
Data is available via: 1KG_ONT_Vienna