A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992308



Internal ID6728270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3216998..3223469hg38UCSC Ensembl
Outerchr11:3238228..3244699hg19UCSC Ensembl
Outerchr11:3194804..3201275hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386472
hg196472
hg186472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563677
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992308
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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