A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116497



Internal ID21299763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16444442..16458123hg38UCSC Ensembl
Innerchr4:16446065..16459746hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3813682
hg1913682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090522
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116497
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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