A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4959n54



Internal ID20138383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23922978..23930631hg38UCSC Ensembl
chr16:23934299..23941952hg19UCSC Ensembl
chr16:23841800..23849453hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg387654
hg197654
hg187654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571695, nsv571699, nsv571700, nsv571701, nsv571694, nsv571693, nsv571698, nsv571702
Samples
Known GenesPRKCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4959n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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