A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118059



Internal ID21301325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7051074..7217794hg38UCSC Ensembl
Innerchr16:7101075..7267795hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38166721
hg19166721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098410
Samplessample105
Known GenesRBFOX1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118059
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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