A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117913



Internal ID21301179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102920371..102928125hg38UCSC Ensembl
Innerchr8:103932599..103940353hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg387755
hg197755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1195n145
Supporting Variantsnssv14085840, nssv14086087, nssv14086008
Samplessample32, sample217, sample194
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117913
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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