A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5087n100



Internal ID22791174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3884069..4180263hg38UCSC Ensembl
chr4:3885796..4181990hg19UCSC Ensembl
chr4:3855594..4232891hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38296195
hg19296195
hg18377298
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012536, nsv1013938
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5087n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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