A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530273



Internal ID306264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25399808..25416000hg38UCSC Ensembl
chr21:26772120..26788312hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3816193
hg1916193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734490
Samples
Known GenesLINC00158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530273
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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