A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994857



Internal ID7079392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95206923..95208667hg38UCSC Ensembl
Innerchr11:94940087..94941831hg19UCSC Ensembl
Innerchr11:94579735..94581479hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381745
hg191745
hg181745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587236
SamplesHuRef
Known GenesSESN3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994857
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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