A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733594



Internal ID157260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62652411..62652466hg38UCSC Ensembl
chr20:61283763..61283818hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521305
Supporting Variants
Samples
Known GenesSLCO4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733594
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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