A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702199



Internal ID15092165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73865809..74556070hg38UCSC Ensembl
Innerchr4:74731526..75421787hg19UCSC Ensembl
Innerchr4:74950390..75640651hg18UCSC Ensembl
Innerchr4:75096561..75786822hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38690262
hg19690262
hg18690262
hg17690262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525980
Supporting Variants
Samples
Known GenesAREG, CXCL1, CXCL2, CXCL3, CXCL5, EPGN, EREG, MTHFD2L, PF4, PPBP, PPBPP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702199
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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