A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616178



Internal ID18914459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5346091..5508108hg38UCSC Ensembl
Innerchr4:5347818..5509835hg19UCSC Ensembl
Innerchr4:5398719..5560736hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38162018
hg19162018
hg18162018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010013
Supporting Variants
Samples
Known GenesSTK32B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616178
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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