A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113500



Internal ID21296766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24230725..24345503hg38UCSC Ensembl
Innerchr1:24557215..24671993hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38114779
hg19114779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103792
Samplessample5
Known GenesGRHL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113500
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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