A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110489



Internal ID21293755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66517104..66527034hg38UCSC Ensembl
Innerchr4:67382822..67392752hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg389931
hg199931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv884n145
Supporting Variantsnssv14093624
Samplessample327
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110489
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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