A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008136



Internal ID7073230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:952159..952859hg38UCSC Ensembl
Innerchr17:855399..856099hg19UCSC Ensembl
Innerchr17:802149..802849hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38701
hg19701
hg18701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586217
SamplesHuRef
Known GenesNXN
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008136
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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