A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532899



Internal ID308809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2892820..2895532hg38UCSC Ensembl
chr16:2942821..2945533hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382713
hg192713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705378
Samples
Known GenesFLYWCH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532899
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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