A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633032



Internal ID21825079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50816137..50816769hg38UCSC Ensembl
chr20:49432674..49433306hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053800
Supporting Variants
Samples
Known GenesBCAS4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633032
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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