A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559456



Internal ID18511051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69954471..70146310hg38UCSC Ensembl
Innerchr16:69988374..70180213hg19UCSC Ensembl
Innerchr16:68545875..68737714hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38191840
hg19191840
hg18191840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059337
Supporting Variants
Samples
Known GenesCLEC18A, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559456
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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