A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792476



Internal ID19174734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65794402..66265561hg38UCSC Ensembl
Innerchr18:63461638..63932798hg19UCSC Ensembl
Innerchr18:61612618..62083778hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38471160
hg19471161
hg18471161
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893118
Supporting Variants
Samples
Known GenesCDH7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=110
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792476
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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