A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861958



Internal ID15809228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82751338..82771779hg38UCSC Ensembl
Innerchr16:82784943..82805384hg19UCSC Ensembl
Innerchr16:81342444..81362885hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3820442
hg1920442
hg1820442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573381
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)nssv861958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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