A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516371



Internal ID292831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87659499..87672995hg38UCSC Ensembl
chr16:87693105..87706601hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3813497
hg1913497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710291
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516371
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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