##fileformat=VCFv4.2
##source=HmnFusion
##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variant">
##INFO=<ID=SOFT,Number=1,Type=String,Description="Indicated from which software is derived">
##INFO=<ID=FROM,Number=.,Type=String,Description="Indicated from which reference is derived">
##INFO=<ID=CONS,Number=.,Type=String,Description="Is a consensus">
##INFO=<ID=VAF,Number=.,Type=Float,Description="Allelic frequence observed">
##INFO=<ID=DP,Number=.,Type=Integer,Description="Approximate read depth across all samples">
##INFO=<ID=SU,Number=.,Type=Integer,Description="Number of pieces of evidence supporting the variant across all samples">
##INFO=<ID=PE,Number=.,Type=Integer,Description="Number of paired-end reads supporting the variant across all samples">
##INFO=<ID=SR,Number=.,Type=Integer,Description="Number of split reads supporting the variant across all samples">
##INFO=<ID=SC,Number=.,Type=Integer,Description="Number of soft clipped reads supporting the variant across all samples">
##ALT=<ID=FUS,Description="Fusion">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=VAF,Number=1,Type=Float,Description="Allelic frequence observed">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth">
##FORMAT=<ID=SU,Number=1,Type=Integer,Description="Number of pieces of evidence supporting the variant">
##FORMAT=<ID=PE,Number=1,Type=Integer,Description="Number of paired-end reads supporting the variant">
##FORMAT=<ID=SR,Number=1,Type=Integer,Description="Number of split reads supporting the variant">
##FORMAT=<ID=SC,Number=1,Type=Integer,Description="Number of soft clipped reads supporting the variant">
