A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089842



Internal ID21284935
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 StatusS
Merged Variantsnsv3116547
Supporting Variants
Samplessample367
Known GenesPAPSS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089842
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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