Population genetics studies, both theoretical and empirical, have primarily focused on sequence variation since the dawn of the discipline in the 1920s, even though genetic structural variation was discovered almost at the same time (McClintock, 1931; Sturtevant, 1913). Among the many great contributions of high-throughput sequencing to biology, the renewed, yet vastly greater, appreciation for structural variation stands out. In recent years, many structural variants (SVs) have been associated with traits involved in speciation and adaptation, highlighting their role in micro-and macroevolutionary processes (Mérot et al., 2020; Wellenreuther et al., 2019). Among SVs, copy number variants (CNVs), which encompass all the SVs in which a sequence varies in number of copies among individuals including duplications, insertions, deletions and transposable elements (TEs), have been linked to adaptation to pollution, pesticides, domestication, and high and low temperatures (Axelsson