A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633820



Internal ID18585415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73908655..74243862hg38UCSC Ensembl
Innerchr4:74774372..75109579hg19UCSC Ensembl
Innerchr4:74993236..75328443hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38335208
hg19335208
hg18335208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004768
Supporting Variants
Samples
Known GenesCXCL2, CXCL3, CXCL5, MTHFD2L, PF4, PPBP, PPBPP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3633820
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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