A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093447



Internal ID21279983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160567721..160707545hg38UCSC Ensembl
Innerchr4:161488873..161628697hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38139825
hg19139825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115525
Supporting Variants
Samplessample291
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093447
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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