A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087499



Internal ID21283873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67338132..67340951hg38UCSC Ensembl
Innerchr8:68250367..68253186hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382820
hg192820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113818
Supporting Variants
Samplessample351
Known GenesARFGEF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087499
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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