A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586188



Internal ID7057570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10324409..10326235hg38UCSC Ensembl
Innerchr21:11186222..11188048hg19UCSC Ensembl
Innerchr21:10208093..10209919hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg381827
hg191827
hg181827
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006557
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586188
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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