A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615191



Internal ID18566786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..88678hg38UCSC Ensembl
Innerchr4:12269..88566hg19UCSC Ensembl
Innerchr4:2269..78566hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3876410
hg1976298
hg1876298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005289
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)nssv3615191
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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