A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436398



Internal ID215015
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 StatusM
Merged Variants
Supporting Variantsnssv16937240
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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