A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525647



Internal ID301799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23793519..23898681hg38UCSC Ensembl
chr20:23774156..23879318hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38105163
hg19105163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731647
Samples
Known GenesCST2, CST5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525647
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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