A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559932



Internal ID18511527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83444272..83477059hg38UCSC Ensembl
Innerchr16:83477877..83510664hg19UCSC Ensembl
Innerchr16:82035378..82068165hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3832788
hg1932788
hg1832788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066832
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)nssv3559932
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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