A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026074



Internal ID18768606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184384963..184780663hg38UCSC Ensembl
Innerchr4:185306117..185701817hg19UCSC Ensembl
Innerchr4:185543111..185938811hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38395701
hg19395701
hg18395701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635612
Samples
Known GenesACSL1, CASP3, CENPU, IRF2, PRIMPOL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026074
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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