A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110924



Internal ID21294190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54183178..54189988hg38UCSC Ensembl
Innerchr19:54687061..54693839hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386811
hg196779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv592n145
Supporting Variantsnssv14101336
Samplessample295
Known GenesMBOAT7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110924
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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