A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111171



Internal ID21294437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102922046..102928125hg38UCSC Ensembl
Innerchr8:103934274..103940353hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386080
hg196080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085949, nssv14086990
Samplessample60, sample89
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111171
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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