A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116095



Internal ID21299361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79525454..79534818hg38UCSC Ensembl
Innerchr5:78821277..78830641hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg389365
hg199365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109323
Samplessample309
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116095
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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