A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113845



Internal ID21297111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26289562..26295480hg38UCSC Ensembl
Innerchr4:26291184..26297102hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385919
hg195919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv868n145
Supporting Variantsnssv14107302
Samplessample35
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113845
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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