A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116606



Internal ID21299872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55578310..55588944hg38UCSC Ensembl
Innerchr16:55612222..55622856hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3810635
hg1910635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098200
Samplessample1
Known GenesLPCAT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116606
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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