A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725939



Internal ID149605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35712180..35728124hg38UCSC Ensembl
chr20:34300102..34316046hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3815945
hg1915945
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524621
Supporting Variants
Samples
Known GenesRBM39
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725939
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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