A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615259



Internal ID18566854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34614..62222hg38UCSC Ensembl
Innerchr4:34614..62114hg19UCSC Ensembl
Innerchr4:24614..52114hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3827609
hg1927501
hg1827501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005209
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)nssv3615259
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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