A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857760



Internal ID15805030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57092295..57092959hg38UCSC Ensembl
Innerchr16:57126207..57126871hg19UCSC Ensembl
Innerchr16:55683708..55684372hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38665
hg19665
hg18665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572708
Supporting Variants
Samples
Known GenesCPNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv857760
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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