A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559854



Internal ID18511449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82729124..82755296hg38UCSC Ensembl
Innerchr16:82762729..82788901hg19UCSC Ensembl
Innerchr16:81320230..81346402hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3826173
hg1926173
hg1826173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064438
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559854
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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