A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089691



Internal ID21269196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36398581..36402414hg38UCSC Ensembl
Innerchr9:36398578..36402411hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383834
hg193834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114519
Supporting Variants
Samplessample136
Known GenesRNF38
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089691
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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