A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615167



Internal ID18566762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..80405hg38UCSC Ensembl
Innerchr4:12269..80298hg19UCSC Ensembl
Innerchr4:2269..70298hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3868137
hg1968030
hg1868030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000888
Supporting Variants
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3615167
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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