A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223569



Internal ID22367296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81642132..81646246hg38UCSC Ensembl
chr16:81675737..81679851hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384115
hg194115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380791
SamplesNA19239
Known GenesCMIP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223569
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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