A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406123



Internal ID22463993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26348505..26348626hg38UCSC Ensembl
chr22:26744471..26744592hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947677
Supporting Variants
Samples
Known GenesSEZ6L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406123
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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