A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7528619



Internal ID10460215
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 StatusS
Merged Variantsesv3259052
Supporting Variants
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7528619
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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