A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047482



Internal ID21956715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32521559..32521693hg38UCSC Ensembl
chr22:32917546..32917680hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640885
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047482
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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