A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110219



Internal ID21293485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:23172606..23174988hg38UCSC Ensembl
Innerchr18:20752570..20754952hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099354
Samplessample172
Known GenesCABLES1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110219
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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