A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478469



Internal ID256024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33609521..33609595hg38UCSC Ensembl
chr10:33898449..33898523hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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