A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260517



Internal ID20469735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26311403..26311403hg38UCSC Ensembl
chr21:27683722..27683722hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260517
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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