A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989743



Internal ID7076328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50926732..50936025hg38UCSC Ensembl
Innerchr17:49004093..49013386hg19UCSC Ensembl
Innerchr17:46359092..46368385hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg389294
hg199294
hg189294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv69e180
Supporting Variantsessv3586275
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989743
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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