A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521327



Internal ID297623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58933889..58941359hg38UCSC Ensembl
chr16:58967793..58975263hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387471
hg197471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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