A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562121



Internal ID335080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19541073..19570966hg38UCSC Ensembl
chr22:19528596..19558489hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3829894
hg1929894
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727645
Samples
Known GenesLINC00895
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562121
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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