A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731641



Internal ID155307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23751162..23826964hg38UCSC Ensembl
chr20:23731799..23807601hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3875803
hg1975803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530305
Supporting Variants
Samples
Known GenesCST2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731641
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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