A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv854132



Internal ID16148088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23145653..23149484hg38UCSC Ensembl
Innerchr16:23156974..23160805hg19UCSC Ensembl
Innerchr16:23064475..23068306hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383832
hg193832
hg183832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571674
Supporting Variants
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv854132
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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