EVAapplication/xmlftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chrX.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chrY.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr15.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr14.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr6.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr11.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr7.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr12.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr8.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr5.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr13.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr10.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr16.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr3.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr9.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr4.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr17.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr19.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr18.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr20.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr2.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr1.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr22.snvs.r1.EVA.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB8650/genomedk.chr21.snvs.r1.EVA.vcf.gzprimaryOK2000000Whole Genome SequencingGenomicsTechnical University of Denmark; Aarhus University; Copenhagen University; BGI-EuropeIllumina HiSeq 2500Homo Sapienshttps://www.ebi.ac.uk/eva/?eva-study=PRJEB8650EVAReleased, Single Nucleotide Variant, snv_variant, Discharged, Patient Discharge, Single Nucleotide Variants., Releasing, Discharge, Discharge from Healthcare Facility, Release Determination, snv variant, SNV, ReleaseCATCH22, DGS, VCFS, TBX1C, CAFS, TGA., VCF, CTHM, DGCR, DORV0falseGenomeDK Release 1 SNV callsThis is an aggregate vcf of GATK SNV calls from 10 trios sequenced to high depth from the first phase Danish Pangenome project2015-02-25PRJEB86509606