A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792353



Internal ID18820787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4425743..4518688hg38UCSC Ensembl
Innerchr18:4425743..4518688hg19UCSC Ensembl
Innerchr18:4415743..4508688hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3892946
hg1992946
hg1892946
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893066
Supporting Variants
Samples
Known GenesDLGAP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792353
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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