A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205890



Internal ID20772930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18681901..18708700hg38UCSC Ensembl
chr21:20054219..20081018hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3826800
hg1926800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205890
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01597


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