A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115668



Internal ID21298934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12943421..12949120hg38UCSC Ensembl
Innerchr4:12945045..12950744hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv857n145
Supporting Variantsnssv14089301
Samplessample110
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115668
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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