A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564119



Internal ID7035219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5737008..5743849hg38UCSC Ensembl
Outerchr11:5758238..5765079hg19UCSC Ensembl
Outerchr11:5714814..5721655hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386842
hg196842
hg186842
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989880
Supporting Variants
SamplesHuRef
Known GenesOR56B1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564119
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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