SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population

The data consists of: - Table S1. The haplogroup breakdown for the 934 SweGen haplotypes included in the final mitochondrial genome dataset. - Figure S1. Graphical description of the average read depths observed in the SweGen dataset. - Figure S2. The distribution of read depth for the 16,569 positions of the mitochondrial genome based on the average observed in a subset of 100 representative SweGen haplotypes. - Figure S3. The box-and-whisker plot presents the distribution of average variant frequency for each coverage classification group. The dataset was originally published in DiVA and moved to SND in 2024.