A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861698



Internal ID16155654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79971745..80098047hg38UCSC Ensembl
Innerchr16:80005642..80131944hg19UCSC Ensembl
Innerchr16:78563143..78689445hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38126303
hg19126303
hg18126303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573294
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)nssv861698
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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