A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590981



Internal ID21539553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45671473..45671624hg38UCSC Ensembl
chr22:46067353..46067504hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125591
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590981
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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