A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088805



Internal ID21285917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117704388..117737283hg38UCSC Ensembl
Innerchr9:120466666..120499561hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3832896
hg1932896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112919
Supporting Variants
Samplessample380
Known GenesTLR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088805
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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