A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096486



Internal ID21281204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70132279..70243617hg38UCSC Ensembl
Innerchr16:70166182..70277520hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38111339
hg19111339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111407
Supporting Variants
Samplessample309
Known GenesCLEC18C, LOC100506060, PDPR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096486
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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