A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114928



Internal ID21298194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:51975910..51980635hg38UCSC Ensembl
Innerchr4:52842076..52846801hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg384726
hg194726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094714
Samplessample361
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114928
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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