A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537896



Internal ID21862251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51607711..51607789hg38UCSC Ensembl
chr3:51641727..51641805hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994132
Supporting Variants
Samples
Known GenesRAD54L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537896
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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