A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642489



Internal ID21834536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45594946..45594946hg38UCSC Ensembl
chr21:47014860..47014860hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642489
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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