A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116547



Internal ID21299813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87666391..87676279hg38UCSC Ensembl
Innerchr10:89426148..89436036hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg389889
hg199889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089842
Samplessample367
Known GenesPAPSS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116547
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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