A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990585



Internal ID7076716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:22443534..22451600hg38UCSC Ensembl
Outerchr11:22465080..22473146hg19UCSC Ensembl
Outerchr11:22421656..22429722hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg388067
hg198067
hg188067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564995
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990585
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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