A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587085



Internal ID6711781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1884569..1886410hg38UCSC Ensembl
Innerchr11:1905799..1907640hg19UCSC Ensembl
Innerchr11:1862375..1864216hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381842
hg191842
hg181842
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1011285
Supporting Variants
SamplesHuRef
Known GenesLSP1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587085
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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