A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727968



Internal ID151634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23255029..23255065hg38UCSC Ensembl
chr22:23597216..23597252hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536354
Supporting Variants
Samples
Known GenesBCR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727968
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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