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