A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000794



Internal ID7065924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:107360721..107378451hg38UCSC Ensembl
Outerchr11:107231447..107249177hg19UCSC Ensembl
Outerchr11:106736657..106754387hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3817731
hg1917731
hg1817731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564879
SamplesHuRef
Known GenesCWF19L2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000794
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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