A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv854172



Internal ID15801442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23922978..23928626hg38UCSC Ensembl
Innerchr16:23934299..23939947hg19UCSC Ensembl
Innerchr16:23841800..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 StatusS
Merged Variantsnsv571692
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)nssv854172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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