A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110708



Internal ID21293974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51831178..51833470hg38UCSC Ensembl
Innerchr17:49908538..49910830hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg382293
hg192293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098585
Samplessample361
Known GenesCA10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110708
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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