nstd204 (Chen et al. 2021)
- Organism:
- Human
- Study Type:
- Collection
- Submitter:
- Lei Chen
- Description:
- Structural variation (SV) callsets were generated from whole genome sequencing data of 4,848 Finnish individuals and are composed of 129,166 high-confidence autosome SVs detected by three SV calling pipelines: LUMPY, GenomeSTRiP and CNVnator. All genomes were sequenced at >20x coverage on the Illumina HiSeq X or NovaSeq platforms with paired-end 150bp reads. In each callset, site-level SV data are available with frequency information. More information can be found at Chen et al., biorxiv (2020). See Variant Summary counts for nstd204 in dbVar Variant Summary.
- Publication(s):
- Chen et al. 2021