A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115692



Internal ID21298958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69842731..69846231hg38UCSC Ensembl
Innerchr9:72457647..72461147hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088850
Samplessample402
Known GenesC9orf135
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115692
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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