A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116235



Internal ID21299501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14698101..14779266hg38UCSC Ensembl
Innerchr9:14698099..14779264hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3881166
hg1981166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089469
Samplessample43
Known GenesCER1, FREM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116235
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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