A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790218



Internal ID19168261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5286432..5362401hg38UCSC Ensembl
Innerchr4:5288159..5364128hg19UCSC Ensembl
Innerchr4:5339060..5415029hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3875970
hg1975970
hg1875970
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893864
Supporting Variants
Samples
Known GenesSTK32B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790218
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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