A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097908



Internal ID21287632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11913152..11917058hg38UCSC Ensembl
Innerchr16:12007009..12010915hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383907
hg193907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118335
Supporting Variants
Samplessample404
Known GenesGSPT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097908
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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