A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206010



Internal ID20773050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25522561..25545023hg38UCSC Ensembl
chr21:26894873..26917335hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3822463
hg1922463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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