A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113925



Internal ID21297191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2748509..2755029hg38UCSC Ensembl
Innerchr5:2748623..2755143hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082692
Samplessample400
Known GenesC5orf38, IRX2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113925
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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