A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725925



Internal ID149591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35564372..35564522hg38UCSC Ensembl
chr20:34152140..34152439hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38151
hg19300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725925
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.992156


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