VCFheader

VCF Header Report

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Switzerland Omics

Input source
simple.vcf
Fileformat
VCFv4.3
File date
20090805
Source
myImputationProgramV3.1
Reference
file:///seq/references/1000GenomesPilot-NCBI36.fasta
Samples
3

Contigs

1 contig declared in the header. Showing the first 1. Contig lengths provided for 1 of 1. Assembly labels provided for 1 of 1. MD5 values provided for 1 of 1. Example ID: 20.

IDlengthassemblymd5speciestaxonomy
2062435964B36f126cdf8a6e0c7f379d618ff66beb2daHomo sapiensx

FILTER definitions

IDDescription
q10Quality below 10
s50Less than 50% of samples have data

ALT definitions

None

INFO fields

IDTypeNumberDescription
NSInteger1Number of Samples With Data
DPInteger1Total Depth
AFFloatAAllele Frequency
AAString1Ancestral Allele
DBFlag0dbSNP membership, build 129
H2Flag0HapMap2 membership
Hover for a quick summary. Click a term to read the full available definition.

FORMAT fields

IDTypeNumberDescription
GTString1Genotype
GQInteger1Genotype Quality
DPInteger1Read Depth
HQInteger2Haplotype Quality
FORMAT keys use genotype-key definitions from the VCF specification. Hover for a quick summary. Click a term to read the full available definition.

Other header entries

None

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Definition

Generated with VCFheader, a free and open-source tool created by Switzerland Omics. Use of the software and generated reports is permitted, including in commercial settings. Attribution identifying Switzerland Omics as the creator should be retained where reasonably practicable, but does not imply endorsement. Switzerland Omics® is a registered trade mark. Further information: https://switzerlandomics.ch. VCF specification references in this report relate to samtools and the broader HTS specifications ecosystem and are distributed under the MIT/Expat Licence by Genome Research Ltd. Source: https://github.com/samtools/samtools. Further reading on HTS and file format specifications: https://www.htslib.org/doc/#file-formats.