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Human Genetic Variation Database
version.2.10
Release: 2017.02.02
Last Update of this note: 2016.02.02
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Japanese Genetic Variation Consortium
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What's new
    + version.2.10 (2017.02.02)
        + Exome table
        	+ DBexome20161214.tab	: Merged data
		+ Genotype counts of indel sites (KU, UT, YCU) were fixed.

Change log
    + version.2.00 (2016.07.19)
        + Exome table
        	+ DBexome20160412.tab	: Merged data
		+ Genotype counts of monomorphic sites (KU, UT, YCU) were added.
    + version.1.42 (2014.06.17)
        + Exome table
        	+ DBexome20131010.tab	: Merged data
		+ Genotype counts were added.
    + version.1.41 (2013.11.13)
        + Exome table
        	+ DBexome20131010.tab	: Merged data
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< Database tables >

1. Exome table
    ---------------------------------------------------------------------------------------------------------------------
      Chr | Position | rsID_freq | Ref | Alt | #Sample | Filter | Mean_depth | SD_depth | RR | RA | AA | NR | NA | Gene
    ---------------------------------------------------------------------------------------------------------------------
        Chr		: Chromosome
        Position	: Position
        rsID_freq	: dbSNP rsID / known frequency
        Ref		: Reference allele
        Alt		: Alternative allele
        #Sample		: Number of samples covered
        Filter		: Filtering status
        Mean_depth	: Mean of sample read depth
        SD_depth	: Standard deviation of sample read depth
        RR		: Number of Ref/Ref genotype
        RA		: Number of Ref/Alt genotype
        AA		: Number of Alt/Alt genotype
        NR		: Number of reference allele
        NA		: Number of alternative allele
        Gene		: Gene symbol

    + position information is based on Build 37