A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101364



Internal ID21281051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33372902..33376313hg38UCSC Ensembl
Innerchr19:33863808..33867219hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383412
hg193412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116409
Supporting Variants
Samplessample306
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101364
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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