A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616037



Internal ID18567632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..115411hg38UCSC Ensembl
Innerchr4:68809..115290hg19UCSC Ensembl
Innerchr4:58809..105290hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3846495
hg1946482
hg1846482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004722
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)nssv3616037
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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