A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999138



Internal ID7064774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93135341..93142857hg38UCSC Ensembl
Outerchr11:92868507..92876023hg19UCSC Ensembl
Outerchr11:92508155..92515671hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387517
hg197517
hg187517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565682
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999138
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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