A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733423



Internal ID157089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60331431..60331527hg38UCSC Ensembl
chr20:58906489..58906585hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.076022


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