A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009476



Internal ID7073883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:70225386..70238369hg38UCSC Ensembl
Outerchr11:70071492..70084475hg19UCSC Ensembl
Outerchr11:69749140..69762123hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3812984
hg1912984
hg1812984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565636
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009476
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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