A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586653



Internal ID7058035
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992072
Supporting Variants
SamplesHuRef
Known GenesMRGPRX1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586653
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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