A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5869n100



Internal ID20157485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149649..395798hg38UCSC Ensembl
chr6:149649..395798hg19UCSC Ensembl
chr6:94649..340798hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38246150
hg19246150
hg18246150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026847, nsv1025116
Samples
Known GenesDUSP22, IRF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5869n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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