A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117954



Internal ID21301220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4209169..4235365hg38UCSC Ensembl
Innerchr3:4250853..4277049hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3826197
hg1926197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv744n145
Supporting Variantsnssv14104244
Samplessample41
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117954
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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