A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089064



Internal ID21291796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69089363..69091442hg38UCSC Ensembl
Innerchr10:70849119..70851198hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114345
Supporting Variants
Samplessample79
Known GenesSRGN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089064
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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