A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289513



Internal ID20498731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16397955..16397955hg38UCSC Ensembl
chr21:17770275..17770275hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764636
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289513
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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