A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4958n54



Internal ID20138382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23922978..23928626hg38UCSC Ensembl
chr16:23934299..23939947hg19UCSC Ensembl
chr16:23841800..23847448hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385649
hg195649
hg185649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571690, nsv571689, nsv571691, nsv571692, nsv571697
Samples
Known GenesPRKCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4958n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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