A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856477



Internal ID15803747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46385922..46498901hg19UCSC Ensembl
Innerchr16:44943423..45056402hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg19112980
hg18112980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572452
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv856477
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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