A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053048



Internal ID21962282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45247270..45257781hg38UCSC Ensembl
chr22:45643151..45653662hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3810512
hg1910512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053048
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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