A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111537



Internal ID21294803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108178749..108192135hg38UCSC Ensembl
Innerchr4:109099905..109113291hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3813387
hg1913387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107653
Samplessample93
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111537
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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