A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096410



Internal ID21278672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86606354..86628511hg38UCSC Ensembl
Innerchr16:86639960..86662117hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822158
hg1922158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112149
Supporting Variants
Samplessample272
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096410
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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