A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727991



Internal ID151657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23574114..23574192hg38UCSC Ensembl
chr22:23916301..23916379hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147454
Supporting Variants
Samples
Known GenesIGLL1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727991
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.151577


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