A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738129



Internal ID18689724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3899113..4190525hg38UCSC Ensembl
Innerchr4:3900840..4192252hg19UCSC Ensembl
Innerchr4:3870638..4243153hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38291413
hg19291413
hg18372516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015133
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)nssv3738129
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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