A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088117



Internal ID21283427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104661469..104677588hg38UCSC Ensembl
Innerchr9:107423750..107439869hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3816120
hg1916120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117128
Supporting Variants
Samplessample344
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088117
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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