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