A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204219



Internal ID20771259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5240466..5246597hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.99775


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