A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088242



Internal ID21286316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36989115..36992486hg38UCSC Ensembl
Innerchr8:36846633..36850004hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383372
hg193372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115732
Supporting Variants
Samplessample386
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088242
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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