A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117861



Internal ID21301127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140009887..140014441hg38UCSC Ensembl
Innerchr4:140931041..140935595hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg384555
hg194555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092131
Samplessample217
Known GenesMAML3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117861
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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