A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115193



Internal ID21298459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19072487..19450514hg38UCSC Ensembl
Innerchr5:19072596..19450623hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38378028
hg19378028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv968n145
Supporting Variantsnssv14109208
Samplessample274
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115193
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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