A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042173



Internal ID21951494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31974325..31976412hg38UCSC Ensembl
chr22:32370312..32372399hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042173
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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