A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589422



Internal ID21537986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48290206..48290296hg38UCSC Ensembl
chr22:48686018..48686108hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137607
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589422
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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