A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5090n100



Internal ID22791177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3926160..4205592hg38UCSC Ensembl
chr4:3927887..4207319hg19UCSC Ensembl
chr4:3978814..4258220hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38279433
hg19279433
hg18279407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006189, nsv1014368
Samples
Known GenesFAM86EP, OTOP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5090n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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