{"datasetId":"6e340c4d1e333c7a676b1710d2e3953c","name":"1000 Genomes phase3:GRCh37","id":"3","referenceSetId":"GRCh37","metadata":[{"id":"CIEND","info":{},"description":"Confidence interval around END for imprecise variants","number":"2","key":"INFO","type":"Integer"},{"info":{},"id":"CIPOS","number":"2","key":"INFO","description":"Confidence interval around POS for imprecise variants","type":"Integer"},{"description":"Source call set.","number":"1","key":"INFO","type":"String","id":"CS","info":{}},{"id":"END","info":{},"description":"End coordinate of this variant","number":"1","key":"INFO","type":"Integer"},{"id":"IMPRECISE","info":{},"type":"Flag","description":"Imprecise structural variation","key":"INFO","number":"0"},{"id":"MC","info":{},"description":"Merged calls.","number":".","key":"INFO","type":"String"},{"info":{},"id":"MEINFO","type":"String","number":"4","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","description":"Mitochondrial end coordinate of inserted sequence","key":"INFO","number":"1","id":"MEND","info":{}},{"id":"MLEN","info":{},"type":"Integer","description":"Estimated length of mitochondrial insert","key":"INFO","number":"1"},{"description":"Mitochondrial start coordinate of inserted sequence","number":"1","key":"INFO","type":"Integer","id":"MSTART","info":{}},{"info":{},"id":"SVLEN","key":"INFO","number":".","description":"Difference in length between REF and ALT alleles","type":"Integer"},{"id":"SVTYPE","info":{},"type":"String","description":"Type of structural variant","number":"1","key":"INFO"},{"type":"String","description":"Precise Target Site Duplication for bases, if unknown, value will be NULL","number":"1","key":"INFO","id":"TSD","info":{}},{"description":"Total number of alternate alleles in called genotypes","number":"A","key":"INFO","type":"Integer","id":"AC","info":{}},{"id":"AF","info":{},"description":"Estimated allele frequency in the range (0,1)","key":"INFO","number":"A","type":"Float"},{"description":"Number of samples with data","number":"1","key":"INFO","type":"Integer","id":"NS","info":{}},{"type":"Integer","number":"1","key":"INFO","description":"Total number of alleles in called genotypes","info":{},"id":"AN"},{"description":"Allele frequency in the EAS populations calculated from AC and AN, in the range (0,1)","key":"INFO","number":"A","type":"Float","id":"EAS_AF","info":{}},{"info":{},"id":"EUR_AF","key":"INFO","number":"A","description":"Allele frequency in the EUR populations calculated from AC and AN, in the range (0,1)","type":"Float"},{"id":"AFR_AF","info":{},"description":"Allele frequency in the AFR populations calculated from AC and AN, in the range (0,1)","key":"INFO","number":"A","type":"Float"},{"info":{},"id":"AMR_AF","type":"Float","number":"A","key":"INFO","description":"Allele frequency in the AMR populations calculated from AC and AN, in the range (0,1)"},{"description":"Allele frequency in the SAS populations calculated from AC and AN, in the range (0,1)","key":"INFO","number":"A","type":"Float","id":"SAS_AF","info":{}},{"id":"DP","info":{},"type":"Integer","description":"Total read depth","number":"1","key":"INFO"},{"type":"String","description":"dbSNP ssID of the allele","key":"INFO","number":"A","id":"ssID","info":{}},{"type":"String","number":"1","key":"FORMAT","description":"Genotype","info":{},"id":"GT"}]}