A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730826



Internal ID154492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10323921..10324068hg38UCSC Ensembl
chr20:10304569..10304716hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533037
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.629878


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