A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638344



Internal ID21830391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26348591..26348591hg38UCSC Ensembl
chr22:26744557..26744557hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108744
Supporting Variants
Samples
Known GenesSEZ6L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638344
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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