A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893118



Internal ID19183938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65794402..66265561hg38UCSC Ensembl
Outerchr18:65794402..66265561hg38UCSC Ensembl
Innerchr18:63461638..63932798hg19UCSC Ensembl
Outerchr18:63461638..63932798hg19UCSC Ensembl
Innerchr18:61612618..62083778hg18UCSC Ensembl
Outerchr18:61612618..62083778hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38471160
hg19471161
hg18471161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792476
Samples
Known GenesCDH7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893118
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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