A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5067n100



Internal ID20156683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35822..69821hg38UCSC Ensembl
chr4:35822..69713hg19UCSC Ensembl
chr4:25822..59713hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834000
hg1933892
hg1833892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004146, nsv1002858, nsv1003556
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5067n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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