A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089308



Internal ID21267265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:220108999..220111910hg38UCSC Ensembl
Innerchr1:220282341..220285252hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382912
hg192912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115941
Supporting Variants
Samplessample110
Known GenesIARS2, RNU5F-1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089308
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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