A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559531



Internal ID18511126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70117612..70212424hg38UCSC Ensembl
Innerchr16:70151515..70246327hg19UCSC Ensembl
Innerchr16:68709016..68803828hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3894813
hg1994813
hg1894813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058087
Supporting Variants
Samples
Known GenesCLEC18C, PDPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559531
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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