A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049953



Internal ID21959186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28036602..28039706hg38UCSC Ensembl
chr22:28432590..28435694hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383105
hg193105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640521
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049953
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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