A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206065



Internal ID20773105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31594142..31610862hg38UCSC Ensembl
chr21:32966455..32983175hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3816721
hg1916721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer