A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114764



Internal ID21298030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65880717..65886938hg38UCSC Ensembl
Innerchr5:65176545..65182766hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg386222
hg196222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv978n145
Supporting Variantsnssv14108412
Samplessample141
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114764
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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