{"metadata":[{"description":"Confidence interval around END for imprecise variants","key":"INFO","type":"Integer","info":{},"number":"2","id":"CIEND"},{"type":"Integer","number":"2","info":{},"id":"CIPOS","description":"Confidence interval around POS for imprecise variants","key":"INFO"},{"key":"INFO","description":"Source call set.","info":{},"number":"1","id":"CS","type":"String"},{"type":"Integer","id":"END","info":{},"number":"1","description":"End coordinate of this variant","key":"INFO"},{"description":"Imprecise structural variation","key":"INFO","type":"Flag","number":"0","info":{},"id":"IMPRECISE"},{"type":"String","info":{},"number":".","id":"MC","description":"Merged calls.","key":"INFO"},{"description":"Mobile element info of the form NAME,START,ENDPOLARITY; If there is only 5' OR 3' support for this call, will be NULL NULL for START and END","key":"INFO","type":"String","info":{},"number":"4","id":"MEINFO"},{"type":"Integer","number":"1","info":{},"id":"MEND","description":"Mitochondrial end coordinate of inserted sequence","key":"INFO"},{"key":"INFO","description":"Estimated length of mitochondrial insert","id":"MLEN","info":{},"number":"1","type":"Integer"},{"description":"Mitochondrial start coordinate of inserted sequence","key":"INFO","type":"Integer","number":"1","info":{},"id":"MSTART"},{"info":{},"number":".","id":"SVLEN","type":"Integer","key":"INFO","description":"Difference in length between REF and ALT alleles"},{"key":"INFO","description":"Type of structural variant","number":"1","info":{},"id":"SVTYPE","type":"String"},{"key":"INFO","description":"Precise Target Site Duplication for bases, if unknown, value will be NULL","number":"1","info":{},"id":"TSD","type":"String"},{"number":"A","info":{},"id":"AC","type":"Integer","key":"INFO","description":"Total number of alternate alleles in called genotypes"},{"info":{},"number":"A","id":"AF","type":"Float","key":"INFO","description":"Estimated allele frequency in the range (0,1)"},{"description":"Number of samples with data","key":"INFO","type":"Integer","id":"NS","info":{},"number":"1"},{"type":"Integer","number":"1","info":{},"id":"AN","description":"Total number of alleles in called genotypes","key":"INFO"},{"description":"Allele frequency in the EAS populations calculated from AC and AN, in the range (0,1)","key":"INFO","type":"Float","info":{},"id":"EAS_AF","number":"A"},{"type":"Float","number":"A","info":{},"id":"EUR_AF","description":"Allele frequency in the EUR populations calculated from AC and AN, in the range (0,1)","key":"INFO"},{"info":{},"number":"A","id":"AFR_AF","type":"Float","key":"INFO","description":"Allele frequency in the AFR populations calculated from AC and AN, in the range (0,1)"},{"description":"Allele frequency in the AMR populations calculated from AC and AN, in the range (0,1)","key":"INFO","type":"Float","info":{},"number":"A","id":"AMR_AF"},{"type":"Float","info":{},"number":"A","id":"SAS_AF","description":"Allele frequency in the SAS populations calculated from AC and AN, in the range (0,1)","key":"INFO"},{"type":"Integer","info":{},"number":"1","id":"DP","description":"Total read depth","key":"INFO"},{"key":"INFO","description":"dbSNP ssID of the allele","info":{},"id":"ssID","number":"A","type":"String"},{"description":"The transformationm for dbSNP results in different POS for the alleles on this line","key":"INFO","type":"Flag","id":"TRANSFORM_TO_DIFFERENT_POS","info":{},"number":"0"},{"type":"Flag","info":{},"number":"0","id":"ASP","description":"Is Assembly specific. This is set if the variant only maps to one assembly (dbSNP flag)","key":"INFO"},{"number":"1","info":{},"id":"WGT","type":"Integer","key":"INFO","description":"Weight, 00 - unmapped, 1 - weight 1, 2 - weight 2, 3 - weight 3 or more (dbSNP flag)"},{"key":"INFO","description":"RS orientation is reversed (dbSNP flag)","info":{},"number":"0","id":"RV","type":"Flag"},{"key":"INFO","description":"rsID to which the remapping of INFO flag WGT relates","info":{},"number":"1","id":"WGT_ref_RS","type":"String"},{"key":"INFO","description":"The REF cannot be resolved between builds","id":"ERR_REF","info":{},"number":"0","type":"Flag"},{"key":"INFO","description":"The REF matched the - strand in GRCh38","info":{},"number":"0","id":"MATCHED_REV","type":"Flag"},{"number":"0","info":{},"id":"MATCHED_FWD","type":"Flag","key":"INFO","description":"The REF matched the + strand in GRCh38"},{"key":"INFO","description":"The REF and ALT have switched between GRCh37 and GRCh38","info":{},"number":"0","id":"SWITCHED_REF","type":"Flag"},{"id":"REF_SWITCHED_TO_NON_PHASE3_ALT","info":{},"number":"0","type":"Flag","key":"INFO","description":"The REF has changed to a non-PHASE3 ALT"},{"info":{},"id":"ALLELES_DIFFERENT_POS","number":"0","type":"Flag","key":"INFO","description":"dbSNP has different POS for ALTS on the same line"},{"description":"An ID has been missed in remapping","key":"INFO","type":"Flag","info":{},"number":"0","id":"MISSED_ID"},{"info":{},"number":"0","id":"MISSED_ALT","type":"Flag","key":"INFO","description":"An ALT has been missed in remapping"},{"info":{},"number":"0","id":"NO_RS_TO_MAP_TO","type":"Flag","key":"INFO","description":"The rs cannot be used to remap"},{"type":"String","info":{},"id":"GT","number":"1","description":"Genotype","key":"FORMAT"}],"referenceSetId":"GRCh38","datasetId":"6e340c4d1e333c7a676b1710d2e3953c","id":"1","name":"1000 Genomes phase3:GRCh38"}