A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451321



Internal ID229506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187744718..187744799hg38UCSC Ensembl
chr3:187462506..187462587hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942688
Samples
Known GenesBCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451321
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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