A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089464



Internal ID21287921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23289386..23296952hg38UCSC Ensembl
Innerchr9:23289384..23296950hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg387567
hg197567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111721
Supporting Variants
Samplessample41
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089464
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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