A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117238



Internal ID21300504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113944467..113949849hg38UCSC Ensembl
Innerchr3:113663314..113668696hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg385383
hg195383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv777n145
Supporting Variantsnssv14107757
Samplessample273
Known GenesGRAMD1C, ZDHHC23
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117238
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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