A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205907



Internal ID20772947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18891793..18921806hg38UCSC Ensembl
chr21:20264111..20294124hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3830014
hg1930014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205907
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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