A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555877



Internal ID329026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48357475..48377091hg38UCSC Ensembl
chr22:48753287..48772903hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3819617
hg1919617
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555877
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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