A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112996



Internal ID21296262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70111585..70243617hg38UCSC Ensembl
Innerchr16:70145488..70277520hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38132033
hg19132033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv452n145
Supporting Variantsnssv14097910
Samplessample404
Known GenesCLEC18C, LOC100506060, PDPR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112996
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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