A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586661



Internal ID6711357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3217492..3222847hg38UCSC Ensembl
Innerchr11:3238722..3244077hg19UCSC Ensembl
Innerchr11:3195298..3200653hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385356
hg195356
hg185356
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006228
Supporting Variants
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586661
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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