A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3259052



Internal ID10932032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3217510..3222858hg38UCSC Ensembl
Outerchr11:3238740..3244088hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385349
hg195349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7528619
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3259052
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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