A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016376



Internal ID18758911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182859067..183262599hg38UCSC Ensembl
Innerchr4:183780220..184183752hg19UCSC Ensembl
Innerchr4:184017214..184420746hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38403533
hg19403533
hg18403533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635603
Samples
Known GenesDCTD, FAM92A1P2, WWC2, WWC2-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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