A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112390



Internal ID21295656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82657316..82658810hg38UCSC Ensembl
Innerchr5:81953135..81954629hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381495
hg191495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv979n145
Supporting Variantsnssv14096779
Samplessample38
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112390
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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