A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636096



Internal ID18587691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152308716..152413464hg38UCSC Ensembl
Innerchr4:153229868..153334616hg19UCSC Ensembl
Innerchr4:153449318..153554066hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38104749
hg19104749
hg18104749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031970
Supporting Variants
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636096
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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