A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738106



Internal ID18689701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3877879..4184322hg38UCSC Ensembl
Innerchr4:3879606..4186049hg19UCSC Ensembl
Innerchr4:3849404..4236950hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38306444
hg19306444
hg18387547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998727
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)nssv3738106
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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