A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559464



Internal ID18511059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69954471..70179129hg38UCSC Ensembl
Innerchr16:69988374..70213032hg19UCSC Ensembl
Innerchr16:68545875..68770533hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38224659
hg19224659
hg18224659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063690
Supporting Variants
Samples
Known GenesCLEC18A, CLEC18C, 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)nssv3559464
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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