A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787944



Internal ID18829322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32107275..32154301hg38UCSC Ensembl
Innerchr5:32107381..32154407hg19UCSC Ensembl
Innerchr5:32143138..32190164hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3847027
hg1947027
hg1847027
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894170
Supporting Variants
Samples
Known GenesGOLPH3, PDZD2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787944
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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