A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114083



Internal ID21297349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89960717..89965637hg38UCSC Ensembl
Innerchr9:92722999..92727919hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384921
hg194921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1244n145
Supporting Variantsnssv14089481, nssv14086918
Samplessample227, sample45
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114083
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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