A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563677



Internal ID6688719
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992308
Supporting Variants
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563677
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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