A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100953



Internal ID21287194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62799676..62803120hg38UCSC Ensembl
Innerchr18:60466909..60470353hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383445
hg193445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112099
Supporting Variants
Samplessample399
Known GenesPHLPP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100953
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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