A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv854185



Internal ID15801455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23922978..23933162hg38UCSC Ensembl
Innerchr16:23934299..23944483hg19UCSC Ensembl
Innerchr16:23841800..23851984hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3810185
hg1910185
hg1810185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571696
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)nssv854185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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