A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086151



Internal ID21276176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18890133..18891494hg38UCSC Ensembl
Innerchr8:18747643..18749004hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110804
Supporting Variants
Samplessample233
Known GenesPSD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086151
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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