A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616138



Internal ID18914419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3870638..4150577hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg18279940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999754
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)nssv3616138
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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