A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594422



Internal ID21543020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32931818..32931894hg38UCSC Ensembl
chr22:33327803..33327879hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123806
SamplesNA24385
Known GenesSYN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594422
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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