A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533558



Internal ID18485153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101824112..101946038hg38UCSC Ensembl
Innerchr14:102290449..102412375hg19UCSC Ensembl
Innerchr14:101360202..101482128hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38121927
hg19121927
hg18121927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038990
Supporting Variants
Samples
Known GenesPPP2R5C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533558
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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