##fileformat=VCFv4.4
##ALT=<ID=INV,Description="Inversion">
##ALT=<ID=INS,Description="Insertion">
##ALT=<ID=DUP,Description="Duplication">
##ALT=<ID=DUP:TANDEM,Description="Tandem Duplication">
##ALT=<ID=DEL,Description="Deletion">
##ALT=<ID=CNV,Description="Copy number variable region">
##INFO=<ID=MATEID,Number=A,Type=String,Description="ID of mate breakend">
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the longest variant described in this record">
##INFO=<ID=CIPOS,Number=.,Type=Integer,Description="Confidence interval around POS for symbolic structural variants">
##INFO=<ID=SVLEN,Number=A,Type=Integer,Description="Length of structural variant">
##INFO=<ID=CILEN,Number=.,Type=Integer,Description="Confidence interval for the SVLEN field">
##INFO=<ID=EVENT,Number=A,Type=String,Description="ID of associated event">
##INFO=<ID=EVENTTYPE,Number=A,Type=String,Description="Type of associated event">
##INFO=<ID=SVCLAIM,Number=A,Type=String,Description="Claim made by the structural variant call. Valid values are D, J, DJ for abundance, adjacency and both respectively">
##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="Imprecise structural variation">
##contig=<ID=chrA,length=1000000>
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##custom_header_field_containing_chr_seq=ATGCGAAAAAAATGT
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	sample
chrA	2	.	TGC	T	.	.	EVENT=DEL_seq	GT	0/1
chrA	2	.	T	<DEL>	.	.	SVLEN=2;SVCLAIM=DJ;EVENT=DEL_symbolic;END=4	GT	0/1
chrA	2	delbp1	T	T[chrA:5[	.	.	MATEID=delbp2;EVENT=DEL_split_bp_cn	GT	0/1
chrA	2	delbp2	A	]chrA:2]A	.	.	MATEID=delbp1;EVENT=DEL_split_bp_cn	GT	0/1
chrA	2	.	T	<DEL>	.	.	SVLEN=2;SVCLAIM=D;EVENT=DEL_split_bp_cn;END=4	GT	0/1
chrA	5	.	G	GAAA	.	.	EVENT=homology_seq	GT	1/1
chrA	5	.	G	<DUP>	.	.	SVLEN=3;CIPOS=0,5;EVENT=homology_dup;END=8	GT	1/1
chrA	14	.	T	<INS>	.	.	IMPRECISE;SVLEN=100;CILEN=-50,50;CIPOS=-10,10;END=14	GT	0/1
chrA	14	.	G	.CCCCCCG	.	.	EVENT=single_breakend	GT	0/1
