A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633226



Internal ID21825273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30652611..30653749hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633226
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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