This collection presents a reanalysis of the sequence data generated by the original 1000 Genomes Project.

The 1000 Genomes Project used primarily a combination of exome and low-coverage sequence data to analyse a panel of 2,504 unrelated individuals in phase three of that project on the GRCh37 reference assembly. That data and analysis is available in our phase three data collection.

This collection realigns and recalls the sequence data from the original project on the GRCh38 assembly. A description of the alignments is given in Zheng-Bradley et al. (2017) and the variant calling is described in Lowy-Gallego et al. (2019).