A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098200



Internal ID21266485
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 StatusS
Merged Variantsnsv3116606
Supporting Variants
Samplessample1
Known GenesLPCAT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098200
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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