A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616163



Internal ID18914444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3926160..4176070hg38UCSC Ensembl
Innerchr4:3927887..4177797hg19UCSC Ensembl
Innerchr4:3978814..4228698hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38249911
hg19249911
hg18249885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006189
Supporting Variants
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616163
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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