A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5892n100



Internal ID22791979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:294274..389630hg38UCSC Ensembl
chr6:294274..389630hg19UCSC Ensembl
chr6:239274..334630hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3895357
hg1995357
hg1895357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024877, nsv1019033, nsv1024084, nsv1034176, nsv1026641, nsv1033616, nsv1015568, nsv1019041, nsv1027914, nsv1022444, nsv1027772, nsv1027450, nsv1022744, nsv1022961
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5892n100
Frequency
Sample Size11257
Observed Gain63
Observed Loss0
Observed Complex0
Frequencyn/a


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