A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981493



Internal ID21890836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161620704..161628292hg38UCSC Ensembl
chr1:161590494..161598082hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387589
hg197589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527125
Samples
Known GenesFCGR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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