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