A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097938



Internal ID21288960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65124544..65138153hg38UCSC Ensembl
Innerchr16:65158447..65172056hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3813610
hg1913610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114878
Supporting Variants
Samplessample424
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097938
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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