A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630889



Internal ID21822936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5235473..5235473hg38UCSC Ensembl
chr20:5216119..5216119hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630889
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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