A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147454



Internal ID346635
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 StatusM
Merged Variants
Supporting Variantsnssv17727991
Samples
Known GenesIGLL1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147454
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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