A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750376



Internal ID20526391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33028665..33028665hg38UCSC Ensembl
chr22:33424650..33424650hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270417
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750376
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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