A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636114



Internal ID18587709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152324311..152392321hg38UCSC Ensembl
Innerchr4:153245463..153313473hg19UCSC Ensembl
Innerchr4:153464913..153532923hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3868011
hg1968011
hg1868011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030237
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)nssv3636114
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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