A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521976



Internal ID298250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2786675..2787461hg38UCSC Ensembl
chr16:2836676..2837462hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706821
Samples
Known GenesPRSS33
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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