A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116787



Internal ID21300053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10108070..10232763hg38UCSC Ensembl
Innerchr4:10109694..10234387hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38124694
hg19124694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094836
Samplessample380
Known GenesWDR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116787
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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