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