A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087973



Internal ID21278826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89960275..89965637hg38UCSC Ensembl
Innerchr9:92722557..92727919hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg385363
hg195363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113209
Supporting Variants
Samplessample274
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087973
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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