A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112001



Internal ID21295267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150948013..151208067hg38UCSC Ensembl
Innerchr4:151869165..152129219hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38260055
hg19260055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094735
Samplessample364
Known GenesLRBA, RPS3A, SH3D19, SNORD73A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112001
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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