A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998783



Internal ID7064536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33807769..33808235hg38UCSC Ensembl
Innerchr10:34096697..34097163hg19UCSC Ensembl
Innerchr10:34136703..34137169hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38467
hg19467
hg18467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586608
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998783
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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