A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv854173



Internal ID15801443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23922978..23929417hg38UCSC Ensembl
Innerchr16:23934299..23940738hg19UCSC Ensembl
Innerchr16:23841800..23848239hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386440
hg196440
hg186440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571693
Supporting Variants
Samples
Known GenesPRKCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv854173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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