A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440736



Internal ID219237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187744562..187744700hg38UCSC Ensembl
chr3:187462350..187462488hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942687
Samples
Known GenesBCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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