A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268484



Internal ID20477702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33001513..33001513hg38UCSC Ensembl
chr20:31589319..31589319hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754910
Supporting Variants
Samples
Known GenesSUN5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268484
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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