A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616182



Internal ID18914463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6372826..6410674hg38UCSC Ensembl
Innerchr4:6374553..6412401hg19UCSC Ensembl
Innerchr4:6425454..6463302hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3837849
hg1937849
hg1837849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008105
Supporting Variants
Samples
Known GenesPPP2R2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616182
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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