Related Experiment Video
Updated: Jan 17, 2026

Incremental Temperature Changes for Maximal Breeding and Spawning in Astyanax mexicanus
Published on: February 14, 2021
High-density LD-based structural variations analysis in ten Native and Mestizo Mexican populations
Adriana Griselda Mateos-Valenzuela1, Mirvana Elizabeth González-Macías2, Carlos Villa-Angulo1
1Laboratory of Bioinformatics and Biophotonics, Engineering Institute, Autonomous University of Baja California, Mexicali, Baja California, México.
Abstract:
The main objective of this study was to perform a genome-wide characterization of Structural Variations (SV) based on the deviation of the expected short-range Linkage Disequilibrium (LD) between Single Nucleotide Polymorphisms (SNPs) in 10 Native and Mestizo Mexican populations. We used a panel of 785,663 SNP genotypes, sampled from 383 individuals, of which 71 belonged to ethnic populations and 312 belonged to mestizo populations. The total number of variations found among all populations was 4,375, involving an average of 19,438 SNPs per population, which corresponds to the 3.14% of the total average of SNPs per population. The mean SV size varied from 2,845-8,646 kb across populations (with a mean SV size of 6,161 kb over all populations) and an average of 50.14 SNPs per SV. By grouping all variations across all populations in the sample we defined 506 regions, from which in 54 (11%) regions the 10 populations coincided. The total number of genes covered by these variations was 8,443. And, from all genes we identified some specifically related to Mexican health, as the genes FTO and ABCA1 associated with obesity, with the adipose tissue function, and with the distribution of fat in Mexican population; the gene ELMO1 associated with the susceptibility to diabetic nephropathy and diabetes type II, among others. In summary, our results add new evidence in support of the hypothesis that SVs based on the deviation of the expected short-range LD between SNPs capture the structure and the demographic history of populations, and represent potential targets for association of SVs with population-specific diseases.
More Related Videos
Related Concept Videos
Genetic Variation
Genes exist in different versions called alleles,...
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Incomplete Dominance
Longitudinal Studies
Three-Dimensional Analysis of Strain
Pedigree Analysis

