A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565086



Internal ID7036186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:8050228..8050991hg38UCSC Ensembl
Outerchr11:8071775..8072538hg19UCSC Ensembl
Outerchr11:8028351..8029114hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387708
hg197708
hg187708
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001231
Supporting Variants
SamplesHuRef
Known GenesTUB
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565086
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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