A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995666



Internal ID7063292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58168350..58168873hg38UCSC Ensembl
Innerchr17:56245711..56246234hg19UCSC Ensembl
Innerchr17:53600710..53601233hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38524
hg19524
hg18524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587175
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995666
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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