A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586158



Internal ID7057540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41847264..41885234hg38UCSC Ensembl
Innerchr10:42355001..42392945hg19UCSC Ensembl
Innerchr10:41674981..41712951hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3837971
hg1937945
hg1837971
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003224
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586158
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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