A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089689



Internal ID21269194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14321648..14323639hg38UCSC Ensembl
Innerchr9:14321647..14323638hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381992
hg191992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115650
Supporting Variants
Samplessample136
Known GenesNFIB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089689
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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