A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616032



Internal ID18567627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66815..143160hg38UCSC Ensembl
Innerchr4:66707..136942hg19UCSC Ensembl
Innerchr4:56707..126942hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3876346
hg1970236
hg1870236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012102
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)nssv3616032
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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