A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515579



Internal ID292060
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 StatusM
Merged Variants
Supporting Variantsnssv17725925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515579
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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