A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997322



Internal ID7081292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21166913..21168368hg38UCSC Ensembl
Innerchr13:21741052..21742507hg19UCSC Ensembl
Innerchr13:20639052..20640507hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381456
hg191456
hg181456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586826
SamplesHuRef
Known GenesSKA3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997322
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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