A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764476



Internal ID16058432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1936174..1942489hg38UCSC Ensembl
Innerchr11:1957404..1963719hg19UCSC Ensembl
Innerchr11:1913980..1920295hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386316
hg196316
hg186316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553061
Supporting Variants
Samples
Known GenesTNNT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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