A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856522



Internal ID16150478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46401993..46464868hg38UCSC Ensembl
Innerchr16:46435905..46498780hg19UCSC Ensembl
Innerchr16:44993406..45056281hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3862876
hg1962876
hg1862876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572463
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)nssv856522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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