A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733409



Internal ID157075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60133731..60146471hg38UCSC Ensembl
chr20:58708787..58721527hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812741
hg1912741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529756
Supporting Variants
Samples
Known GenesLOC284757
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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