A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652641



Internal ID15042607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152334981..152388386hg38UCSC Ensembl
Innerchr4:153256133..153309538hg19UCSC Ensembl
Innerchr4:153475583..153528988hg18UCSC Ensembl
Innerchr4:153613738..153667143hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3853406
hg1953406
hg1853406
hg1753406
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516218
Supporting Variants
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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