A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861988



Internal ID15809258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83759413..83778035hg38UCSC Ensembl
Innerchr16:83793018..83811640hg19UCSC Ensembl
Innerchr16:82350519..82369141hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3818623
hg1918623
hg1818623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573402
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861988
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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