A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111087



Internal ID21294353
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 StatusM
Merged Variants
Supporting Variantsnssv14109408
Samplessample335
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111087
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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