A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732348



Internal ID156014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39251496..39255408hg38UCSC Ensembl
chr20:37880139..37884051hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg383913
hg193913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732348
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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