A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565168



Internal ID7036550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:60803960..60805250hg38UCSC Ensembl
Outerchr11:60571433..60572723hg19UCSC Ensembl
Outerchr11:60328009..60329299hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381291
hg191291
hg181291
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996765
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565168
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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