A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010016



Internal ID7059710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110943310..110950730hg38UCSC Ensembl
Outerchr11:110814034..110821454hg19UCSC Ensembl
Outerchr11:110319244..110326664hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387421
hg197421
hg187421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563625
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010016
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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