A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565351



Internal ID7036733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1928703..1939858hg38UCSC Ensembl
Outerchr11:1949933..1961088hg19UCSC Ensembl
Outerchr11:1906509..1917664hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3817245
hg1917245
hg1817245
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007968
Supporting Variants
SamplesHuRef
Known GenesTNNT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565351
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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