A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861956



Internal ID15809226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82679946..82854026hg38UCSC Ensembl
Innerchr16:82713551..82887631hg19UCSC Ensembl
Innerchr16:81271052..81445132hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38174081
hg19174081
hg18174081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573379
Supporting Variants
Samples
Known GenesCDH13, MIR8058
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861956
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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