A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586858



Internal ID7058240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34700678..34701165hg38UCSC Ensembl
Innerchr21:36072977..36073464hg19UCSC Ensembl
Innerchr21:34994847..34995334hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38488
hg19488
hg18488
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993312
Supporting Variants
SamplesHuRef
Known GenesCLIC6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586858
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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