A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110126



Internal ID21293392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64163879..64169041hg38UCSC Ensembl
Innerchr5:63459706..63464868hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108410
Samplessample141
Known GenesRNF180
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110126
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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