A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098410



Internal ID21266972
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 StatusS
Merged Variantsnsv3118059
Supporting Variants
Samplessample105
Known GenesRBFOX1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098410
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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