A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098219



Internal ID21266577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11910987..11918645hg38UCSC Ensembl
Innerchr16:12004844..12012502hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387659
hg197659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115840
Supporting Variants
Samplessample10
Known GenesGSPT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098219
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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