A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992072



Internal ID7077746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18920312..18943051hg38UCSC Ensembl
Innerchr11:18941859..18964598hg19UCSC Ensembl
Innerchr11:18898435..18921174hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822740
hg1922740
hg1822740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586653
SamplesHuRef
Known GenesMRGPRX1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992072
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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