A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113926



Internal ID21297192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40621453..40627164hg38UCSC Ensembl
Innerchr4:40623470..40629181hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385712
hg195712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089290
Samplessample108
Known GenesRBM47
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113926
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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