Over the past four years, genome-wide studies have uncovered numerous examples of structural variation in the human genome. This includes structural variation that changes copy number, such as deletion and duplication, and structural variation that does not change copy number, such as orientation and positional polymorphism. One region that contains all these types of variation spans the chromosome band 8p23.1. This region has been studied in some depth, and the focus of this review is to examine our current understanding of the variation of this region. We also consider whether this region is a good model for other structurally variable regions in the genome and what the implications of this variation are for clinical studies. Finally, we ...
Abstract Background Several genomes have now been seq...
There is a complex relationship between the evolution of segmental duplications and rearrangements a...
There is a complex relationship between the evolution of segmental duplications and rearrangements a...
Over the past four years, genome-wide studies have uncovered numerous examples of structural variati...
Abstract Background Defensins are important components of innate immunity to combat bacterial and vi...
Genetic variation among individual humans occurs on many different scales, ranging from gross altera...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
BACKGROUND: In highly copy number variable (CNV) regions such as the human defensin gene locus, comp...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
Structural variation includes many different types of chromosomal rearrangement and encompasses mill...
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in...
A key goal of whole-genome sequencing for studies of human genetics is to interrogate all forms of v...
The near completeness of human chromosome sequences is facilitating accurate characterization and as...
Variability in the human genome has far exceeded expectations. In the course of the past three years...
Abstract Background Several genomes have now been seq...
There is a complex relationship between the evolution of segmental duplications and rearrangements a...
There is a complex relationship between the evolution of segmental duplications and rearrangements a...
Over the past four years, genome-wide studies have uncovered numerous examples of structural variati...
Abstract Background Defensins are important components of innate immunity to combat bacterial and vi...
Genetic variation among individual humans occurs on many different scales, ranging from gross altera...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
BACKGROUND: In highly copy number variable (CNV) regions such as the human defensin gene locus, comp...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
Structural variation includes many different types of chromosomal rearrangement and encompasses mill...
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in...
A key goal of whole-genome sequencing for studies of human genetics is to interrogate all forms of v...
The near completeness of human chromosome sequences is facilitating accurate characterization and as...
Variability in the human genome has far exceeded expectations. In the course of the past three years...
Abstract Background Several genomes have now been seq...
There is a complex relationship between the evolution of segmental duplications and rearrangements a...
There is a complex relationship between the evolution of segmental duplications and rearrangements a...