A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205959



Internal ID20772999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:22042048..22054699hg38UCSC Ensembl
chr21:23414367..23427018hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3812652
hg1912652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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