A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524699



Internal ID300895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87693663..87693735hg38UCSC Ensembl
chr16:87727269..87727341hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710298
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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