Data from: The standing pool of genomic structural variation in a natural population of Mimulus guttatus

Major unresolved questions in evolutionary genetics include determining
the contributions of different mutational sources to the total pool of
genetic variation in a species, and understanding how these different
forms of genetic variation interact with natural selection. Recent work
has shown that structural variants (insertions, deletions, inversions and
transpositions) are a major source of genetic variation, often
out-numbering single nucleotide variants in terms of total bases affected.
Despite the near ubiquity of structural variants, major questions about
their interaction with natural selection remain. For example, how does the
allele frequency spectrum of structural variants differ when compared to
single nucleotide variants? How often do structural variants affect genes,
and what are the consequences? To begin to address these questions, we
have systematically identified and characterized a large set
submicroscopic insertion and deletion (indel) variants (between 1 kb to
200 kb in length) among ten individuals from a single natural population
of the plant species Mimulus guttatus. After extensive computational
filtering, we focused on a set of 4,142 high-confidence indels that showed
an experimental validation rate of 73%. All but one of these indels were
< 200 kb. While the largest were generally at lower frequencies in
the population, a surprising number of large indels are at intermediate
frequencies. While indels overlapping with genes were much rarer than
expected by chance, nearly 600 genes were affected by an indel. NBS-LRR
defense response genes were the most enriched among the gene families
affected. Most indels associated with genes were rare and appeared to be
under purifying selection, though we do find four high-frequency derived
insertion alleles that show signatures of recent positive selection.