A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564264



Internal ID7035364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:59280440..59282910hg38UCSC Ensembl
Outerchr11:59047913..59050383hg19UCSC Ensembl
Outerchr11:58804489..58806959hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382326
hg192326
hg182326
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003535
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564264
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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