A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109408



Internal ID21282999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:169547792..169567579hg38UCSC Ensembl
Innerchr5:168974796..168994583hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3819788
hg1919788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111087
Supporting Variants
Samplessample335
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109408
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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