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