A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088057



Internal ID21281625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13571254..13576094hg38UCSC Ensembl
Innerchr9:13571253..13576093hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384841
hg194841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112532
Supporting Variants
Samplessample314
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088057
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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