Expand description
Variant record samples key.
Constants§
- Unique identifier of ancestral haplotype (
AHAP
). - Conditional genotype quality (
GQ
). - Confidence interval around copy number (
CICN
). - Expected alternate allele counts (
EC
). - Filter indicating if this genotype was “called” (
FT
). - Read depth for each allele on the forward strand (
ADF
). - Genotype (
GT
). - Copy number genotype for imprecise events (
CN
). - Copy number genotype likelihood for imprecise events (
CNL
). - Copy number posterior probabilities (
CNP
). - Copy number genotype quality for imprecise events (
CNQ
). - Genotype likelihoods (
GL
). - Genotype posterior probabilities (
GP
). - Unique haplotype identifier (
HAP
). - Haplotype quality (
HQ
). - Length of <*> reference block (
LEN
). - 1-based indices into ALT, indicating which alleles are relevant (local) for the current sample (
LAA
). - Local-allele representation of EC (
LEC
). - Local-allele representation of ADF (
LADF
). - Local-allele representation of GL (
LGL
). - Local-allele representation of GP (
LGP
). - Local-allele representation of AD (
LAD
). - Local-allele representation of ADR (
LADR
). - Local-allele representation of PL (
LPL
). - Local-allele representation of PP (
LPP
). - RMS mapping quality (
MQ
). - Phred style probability score that the variant is novel (
NQ
). - Phase set (
PS
). - Phase set list (
PSL
). - Phase set list ordinal (
PSO
). - Phase set list quality (
PSQ
). - Phasing quality (
PQ
). - Read depth (
DP
). - Read depth for each allele (
AD
). - Reserved (
LA
). - Read depth for each allele on the reverse strand (
ADR
). - Phred-scaled genotype likelihoods rounded to the closest integer (
PL
). - Phred-scaled genotype posterior probabilities rounded to the closest integer (
PP
).