A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937240



Internal ID25537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105831840..105831916hg38UCSC Ensembl
chr3:105550684..105550760hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436398
Supporting Variants
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937240
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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