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