A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205933



Internal ID20772973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20878381..20926162hg38UCSC Ensembl
chr21:22250699..22298479hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3847782
hg1947781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205933
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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