# This file was produced by bcftools stats (1.20+htslib-1.20) and can be plotted using plot-vcfstats.
# The command line was: bcftools stats pos_somatic_028.manta_fusion.somatic_sv.scored.vcf.gz
#
# Definition of sets:
# ID [2]id [3]tab-separated file names
ID 0 pos_somatic_028.manta_fusion.somatic_sv.scored.vcf.gz
# SN, Summary numbers:
# number of records .. number of data rows in the VCF
# number of no-ALTs .. reference-only sites, ALT is either "." or identical to REF
# number of SNPs .. number of rows with a SNP
# number of MNPs .. number of rows with a MNP, such as CC>TT
# number of indels .. number of rows with an indel
# number of others .. number of rows with other type, for example a symbolic allele or
# a complex substitution, such as ACT>TCGA
# number of multiallelic sites .. number of rows with multiple alternate alleles
# number of multiallelic SNP sites .. number of rows with multiple alternate alleles, all SNPs
#
# Note that rows containing multiple types will be counted multiple times, in each
# counter. For example, a row with a SNP and an indel increments both the SNP and
# the indel counter.
#
# SN [2]id [3]key [4]value
SN 0 number of samples: 2
SN 0 number of records: 1514
SN 0 number of no-ALTs: 0
SN 0 number of SNPs: 0
SN 0 number of MNPs: 0
SN 0 number of indels: 427
SN 0 number of others: 406
SN 0 number of multiallelic sites: 0
SN 0 number of multiallelic SNP sites: 0
# TSTV, transitions/transversions:
# TSTV [2]id [3]ts [4]tv [5]ts/tv [6]ts (1st ALT) [7]tv (1st ALT) [8]ts/tv (1st ALT)
TSTV 0 0 0 0.00 0 0 0.00
# SiS, Singleton stats:
# SiS [2]id [3]allele count [4]number of SNPs [5]number of transitions [6]number of transversions [7]number of indels [8]repeat-consistent [9]repeat-inconsistent [10]not applicable
SiS 0 1 0 0 0 427 0 0 427
# AF, Stats by non-reference allele frequency:
# AF [2]id [3]allele frequency [4]number of SNPs [5]number of transitions [6]number of transversions [7]number of indels [8]repeat-consistent [9]repeat-inconsistent [10]not applicable
AF 0 0.000000 0 0 0 427 0 0 427
# QUAL, Stats by quality
# QUAL [2]id [3]Quality [4]number of SNPs [5]number of transitions (1st ALT) [6]number of transversions (1st ALT) [7]number of indels
QUAL 0 . 0 0 0 427
# IDD, InDel distribution:
# IDD [2]id [3]length (deletions negative) [4]number of sites [5]number of genotypes [6]mean VAF
IDD 0 -60 308 0 .
IDD 0 -59 3 0 .
IDD 0 -58 1 0 .
IDD 0 -57 9 0 .
IDD 0 -56 5 0 .
IDD 0 -55 3 0 .
IDD 0 -54 7 0 .
IDD 0 -53 1 0 .
IDD 0 -52 2 0 .
IDD 0 -51 4 0 .
IDD 0 -50 3 0 .
IDD 0 15 1 0 .
IDD 0 16 5 0 .
IDD 0 17 12 0 .
IDD 0 18 1 0 .
IDD 0 19 1 0 .
IDD 0 20 1 0 .
IDD 0 21 2 0 .
IDD 0 23 2 0 .
IDD 0 26 1 0 .
IDD 0 27 4 0 .
IDD 0 28 1 0 .
IDD 0 51 2 0 .
IDD 0 53 1 0 .
IDD 0 54 1 0 .
IDD 0 55 1 0 .
IDD 0 57 2 0 .
IDD 0 59 1 0 .
IDD 0 60 42 0 .
# ST, Substitution types:
# ST [2]id [3]type [4]count
ST 0 A>C 0
ST 0 A>G 0
ST 0 A>T 0
ST 0 C>A 0
ST 0 C>G 0
ST 0 C>T 0
ST 0 G>A 0
ST 0 G>C 0
ST 0 G>T 0
ST 0 T>A 0
ST 0 T>C 0
ST 0 T>G 0
# DP, Depth distribution
# DP [2]id [3]bin [4]number of genotypes [5]fraction of genotypes (%) [6]number of sites [7]fraction of sites (%)