A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115832



Internal ID21299098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:79617436..79619156hg38UCSC Ensembl
Innerchr8:80529671..80531391hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381721
hg191721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085761
Samplessample6
Known GenesSTMN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115832
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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