A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996673



Internal ID7080757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110873209..110874398hg38UCSC Ensembl
Innerchr13:111525556..111526745hg19UCSC Ensembl
Innerchr13:110323557..110324746hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381190
hg191190
hg181190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586808
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996673
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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