A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519250



Internal ID295603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69853069..69861084hg38UCSC Ensembl
chr16:69886972..69894987hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388016
hg198016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707149
Samples
Known GenesWWP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519250
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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