A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104473



Internal ID21291661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85088082..85342824hg38UCSC Ensembl
Innerchr3:85137233..85391974hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38254743
hg19254742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114078
Supporting Variants
Samplessample78
Known GenesCADM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104473
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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