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tigra.vcf
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tigra.vcf
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##fileformat=VCFv4.1
##ALT=<ID=DEL,Description="Deletion">
##ALT=<ID=DUP,Description="Duplication">
##ALT=<ID=INV,Description="Inversion">
##ALT=<ID=TRA,Description="Translocation">
##ALT=<ID=INS,Description="Insertion">
##INFO=<ID=CIEND,Number=2,Type=Integer,Description="PE confidence interval around END">
##INFO=<ID=CIPOS,Number=2,Type=Integer,Description="PE confidence interval around POS">
##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="">
##INFO=<ID=PRECISE,Number=0,Type=Flag,Description="Precise structural variation">
##INFO=<ID=SOMATIC,Number=0,Type=Flag,Description="">
##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variant">
##INFO=<ID=CHR2,Number=1,Type=String,Description="">
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the structural variant">
##INFO=<ID=SVLEN,Number=1,Type=Integer,Description="">
##INFO=<ID=MICRO,Number=1,Type=String,Description="">
##INFO=<ID=TEMPLATE,Number=1,Type=String,Description="">
##INFO=<ID=NONTEMPLATE,Number=1,Type=String,Description="">
##INFO=<ID=CTG,Number=1,Type=String,Description="">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT SAMPLE