A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101296



Internal ID21279467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55591595..55606689hg38UCSC Ensembl
Innerchr19:56102961..56118055hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815095
hg1915095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115592
Supporting Variants
Samplessample283
Known GenesFIZ1, ZNF524
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101296
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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