A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114145



Internal ID21297411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71564762..71723971hg38UCSC Ensembl
Innerchr18:69231998..69391207hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38159210
hg19159210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099490
Samplessample76
Known GenesLOC100505776
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114145
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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