A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005053



Internal ID7070149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50927121..50935993hg38UCSC Ensembl
Innerchr17:49004482..49013354hg19UCSC Ensembl
Innerchr17:46359481..46368353hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg388873
hg198873
hg188873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv69e180
Supporting Variantsessv3586938
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005053
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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