A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616164



Internal ID18914445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3939505..4205592hg38UCSC Ensembl
Innerchr4:3941232..4207319hg19UCSC Ensembl
Innerchr4:3992159..4258220hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38266088
hg19266088
hg18266062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014368
Supporting Variants
Samples
Known GenesFAM86EP, OTOP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616164
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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