A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523101



Internal ID299347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26171919..26171974hg38UCSC Ensembl
chr21:27544237..27544292hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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