A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111933



Internal ID21295199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163793242..163796520hg38UCSC Ensembl
Innerchr5:163220248..163223526hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383279
hg193279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv999n145
Supporting Variantsnssv14108805, nssv14097369, nssv14096683, nssv14109218
Samplessample100, sample6, sample275, sample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111933
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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