A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098391



Internal ID21292994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86366443..86367875hg38UCSC Ensembl
Innerchr16:86400049..86401481hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381433
hg191433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112296
Supporting Variants
Samplessample95
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098391
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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