File: indel-stats.vcf

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##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##contig=<ID=20,length=81195210>
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths">
##INFO=<ID=CSQ,Number=.,Type=String,Description="Local consequence annotation from BCFtools/csq. Format: '[*]consequence|gene|transcript|biotype[|strand|amino_acid_change|dna_change]'">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	child1	father1	mother1	child2	father2	mother2
20	310	.	T	A,C	.	.	.	GT	1/1	1/1	1/1	1/2	2/1	1/1
20	311	.	T	TA	.	.	.	GT:AD	1/1:0,20	0/0:20,0	0/0:20,0	0/1:10,10	.	0/0:20,0
20	312	.	TAA	T	.	.	CSQ=inframe_deletion|SAMD11|ENST00000420190|protein_coding|+|74EDG>74D|865683AGGATGG>A	GT:AD	0/1:10,10	1/0:10,10	0/0:20,0	0/0:20,0	0/0:20,0	0/0:20,0
20	313	.	A	ATT	.	.	CSQ=frameshift|SAMD11|ENST00000342066|protein_coding|+|333LPPAQA	GT:AD	0/1:10,10	0/0:10,10	0/0:20,0	0/0:20,0	0/0:20,0	0/0:20,0