A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089763



Internal ID21271511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23655569..23658006hg38UCSC Ensembl
Innerchr9:23655567..23658004hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115930
Supporting Variants
Samplessample164
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089763
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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