A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115541



Internal ID21298807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113873301..113876081hg38UCSC Ensembl
Innerchr11:113744023..113746803hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg382781
hg192781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv225n145
Supporting Variantsnssv14091130
Samplessample62
Known GenesUSP28
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115541
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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