In order to explore the diversity and selective signatures of duplication and deletion human copy number variants (CNVs), we sequenced 236 individuals from 125 distinct human populations. We observed that duplications exhibit fundamentally different population genetic and selective signatures than deletions and are more likely to be stratified between human populations. Through reconstruction of the ancestral human genome, we identify megabases of DNA lost in different human lineages and pinpoint large duplications that introgressed from the extinct Denisova lineage now found at high frequency exclusively in Oceanic populations. We find that the proportion of CNV base pairs to single nucleotide variant base pairs is greater among non-Africa...
Thousands of genome segments appear to be present in widely varying copy number in different human g...
Background: Understanding the genetic contribution to phenotype variation of human groups is necessa...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
In order to explore the diversity and selective signatures of duplication and deletion human copy-nu...
In order to explore the diversity and selective signatures of duplication and deletion human copy nu...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among ...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Copy number variation is a dominant contributor to genomic variation and may frequently underlie an ...
The structural diversity of the human genome is much higher than previously assumed although its ful...
Global patterns of Copy Number Variations (CNVs) in chromosomes are required to understand the dynam...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
Copy number variants (CNVs) are subject to stronger selective pressure than single-nucleotide varian...
Despite considerable excitement over the potential functional significance of copy-number variants (...
Thousands of genome segments appear to be present in widely varying copy number in different human g...
Background: Understanding the genetic contribution to phenotype variation of human groups is necessa...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
In order to explore the diversity and selective signatures of duplication and deletion human copy-nu...
In order to explore the diversity and selective signatures of duplication and deletion human copy nu...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among ...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Copy number variation is a dominant contributor to genomic variation and may frequently underlie an ...
The structural diversity of the human genome is much higher than previously assumed although its ful...
Global patterns of Copy Number Variations (CNVs) in chromosomes are required to understand the dynam...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
Copy number variants (CNVs) are subject to stronger selective pressure than single-nucleotide varian...
Despite considerable excitement over the potential functional significance of copy-number variants (...
Thousands of genome segments appear to be present in widely varying copy number in different human g...
Background: Understanding the genetic contribution to phenotype variation of human groups is necessa...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...