A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764477



Internal ID16058433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1936960..1940639hg38UCSC Ensembl
Innerchr11:1958190..1961869hg19UCSC Ensembl
Innerchr11:1914766..1918445hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383680
hg193680
hg183680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553062
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)nssv764477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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