A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089469



Internal ID21289101
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 StatusS
Merged Variantsnsv3116235
Supporting Variants
Samplessample43
Known GenesCER1, FREM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089469
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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