A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007915



Internal ID7073008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110706348..110707743hg38UCSC Ensembl
Innerchr13:111358695..111360090hg19UCSC Ensembl
Innerchr13:110156696..110158091hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381396
hg191396
hg181396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587074
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007915
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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