A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206647



Internal ID20773687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31989565..32018244hg38UCSC Ensembl
chr21:33361878..33390557hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3828680
hg1928680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548788
Supporting Variants
Samples
Known GenesHUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206647
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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