A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894127



Internal ID19185196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11428364..12228903hg38UCSC Ensembl
Outerchr5:11428364..12228903hg38UCSC Ensembl
Innerchr5:11428476..12229015hg19UCSC Ensembl
Outerchr5:11428476..12229015hg19UCSC Ensembl
Innerchr5:11481476..12282015hg18UCSC Ensembl
Outerchr5:11481476..12282015hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38800540
hg19800540
hg18800540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788226
Samples
Known GenesCTNND2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894127
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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