File Info

Filename
Sig_18_tissue_vs_Sig_18_Blood.manta.somatic_sv_custom.ann_snpEff.csv
Full Path
s3://natera-rnd-pltf-dev-nextflow-data-01/users/mipeters/semiproductionize/sarek/698115e9/test_regression_dev_b0193075/reports/raw_qc/snpeff/manta/Sig_18_tissue_vs_Sig_18_Blood/Sig_18_tissue_vs_Sig_18_Blood.manta.somatic_sv_custom.ann_snpEff.csv
Size
1.5 KB
Published
Feb 02, 2026 1:43 PM
# Summary table
Name , Value
Genome , GRCh38.105
Date , 2026-02-02 21:43
SnpEff_version , SnpEff 5.1d (build 2022-04-19 15:49), by Pablo Cingolani
Command_line_arguments , SnpEff GRCh38.105 -csvStats Sig_18_tissue_vs_Sig_18_Blood.manta.somatic_sv_custom.ann_snpEff.csv Sig_18_tissue_vs_Sig_18_Blood.manta.somatic_sv_custom.ann.vcf.gz
Warnings , 0
Number_of_lines_in_input_file, 0
Number_of_variants_before_filter, 0
Number_of_not_variants , 0
Number_of_variants_processed , 0
Number_of_known_variants (i.e. non-empty ID) , 0, 0%
Number_of_effects , 0
Genome_total_length ,63147197748
Genome_effective_length ,0
Change_rate , 0
# Change rate by chromosome
Chromosome , Length , Changes , Change_rate
# Variantss by type
Type , Count , Percent
# Effects by impact
Type , Count , Percent
# Effects by functional class
Type , Count , Percent
Missense_Silent_ratio, 0
# Count by effects
Type , Count , Percent
# Count by genomic region
Type , Count , Percent
# Quality
# InDel lengths
# Base changes
base , A , C , G , T
A , 0 , 0 , 0 , 0
C , 0 , 0 , 0 , 0
G , 0 , 0 , 0 , 0
T , 0 , 0 , 0 , 0
# Ts/Tv summary
Transitions , 0
Transversions , 0
Ts_Tv_ratio , 0
# Ts/Tv : All variants
No results available (empty input?)
# Ts/Tv : Known variants
No results available (empty input?)
# Allele frequency
# Allele frequency : All variants
Values ,
Count ,
# Allele Count
Values ,
Count ,
# Hom/Het table
# Codon change table
codons
# Amino acid change table
aa
# Chromosome change table
97 rows