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