A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719313



Internal ID18670908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22333870..22400207hg38UCSC Ensembl
Innerchr16:22345191..22411528hg19UCSC Ensembl
Innerchr16:22252692..22319029hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3866338
hg1966338
hg1866338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053536
Supporting Variants
Samples
Known GenesCDR2, POLR3E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719313
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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