A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669389



Internal ID15059355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152334981..152378721hg38UCSC Ensembl
Innerchr4:153256133..153299873hg19UCSC Ensembl
Innerchr4:153475583..153519323hg18UCSC Ensembl
Innerchr4:153613738..153657478hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3843741
hg1943741
hg1843741
hg1743741
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)nssv669389
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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