A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008105



Internal ID19097324
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 StatusM
Merged Variants
Supporting Variantsnssv3616182
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)nsv1008105
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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