A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206016



Internal ID20773056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26178976..26192602hg38UCSC Ensembl
chr21:27551295..27564921hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3813627
hg1913627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206016
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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