A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993425



Internal ID21902768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33051058..33051427hg38UCSC Ensembl
chr3:33092550..33092919hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556550
Samples
Known GenesGLB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993425
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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