A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521917



Internal ID298194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9815656..9817781hg38UCSC Ensembl
chr19:9926332..9928457hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721259
Samples
Known GenesFBXL12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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