A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586257



Internal ID7057639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17732951..17736208hg38UCSC Ensembl
Innerchr10:17774950..17778207hg19UCSC Ensembl
Innerchr10:17814956..17818213hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg383258
hg193258
hg183258
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997738
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586257
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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