A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521464



Internal ID297759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34660312..34675135hg38UCSC Ensembl
chr20:33248116..33262939hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3814824
hg1914824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732116
Samples
Known GenesPIGU
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521464
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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