A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116153



Internal ID21299419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:91630957..91637925hg38UCSC Ensembl
Innerchr5:90926774..90933742hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386969
hg196969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108853
Samplessample173
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116153
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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