A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117406



Internal ID21300672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69840466..69844801hg38UCSC Ensembl
Innerchr9:72455382..72459717hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg384336
hg194336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1237n145
Supporting Variantsnssv14089667
Samplessample124
Known GenesC9orf135
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117406
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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