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