A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100451



Internal ID21273137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33371984..33376074hg38UCSC Ensembl
Innerchr19:33862890..33866980hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384091
hg194091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116344
Supporting Variants
Samplessample188
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100451
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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