A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006557



Internal ID7071651
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586188
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006557
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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