A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616145



Internal ID18567740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3899113..4180263hg38UCSC Ensembl
Innerchr4:3900840..4181990hg19UCSC Ensembl
Innerchr4:3870638..4232891hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38281151
hg19281151
hg18362254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010973
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)nssv3616145
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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