A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008099



Internal ID7073193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39360252..39361396hg38UCSC Ensembl
Innerchr13:39934389..39935533hg19UCSC Ensembl
Innerchr13:38832389..38833533hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381145
hg191145
hg181145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587068
SamplesHuRef
Known GenesLHFP
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008099
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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