A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586217



Internal ID7057599
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008136
Supporting Variants
SamplesHuRef
Known GenesNXN
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586217
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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