A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518124



Internal ID294521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80833779..80959539hg38UCSC Ensembl
chr16:80867676..80993436hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38125761
hg19125761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518124
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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