A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525621



Internal ID301774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19130224..19148764hg38UCSC Ensembl
chr21:20502542..20521082hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3818541
hg1918541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525621
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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