A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587228



Internal ID6711924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3217540..3222899hg38UCSC Ensembl
Innerchr11:3238770..3244129hg19UCSC Ensembl
Innerchr11:3195346..3200705hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385360
hg195360
hg185360
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006335
Supporting Variants
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587228
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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