A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990794



Internal ID6726760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66643615..66660621hg38UCSC Ensembl
Outerchr11:66411086..66428092hg19UCSC Ensembl
Outerchr11:66167662..66184668hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3817007
hg1917007
hg1817007
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565613
SamplesHuRef
Known GenesRBM14-RBM4, RBM4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990794
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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