A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111483



Internal ID21294749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16072387..16074538hg38UCSC Ensembl
Innerchr4:16074010..16076161hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107335
Samplessample41
Known GenesPROM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111483
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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