A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584825



Internal ID21533369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591590..31591768hg38UCSC Ensembl
chr22:31987576..31987754hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122403
SamplesNA12878
Known GenesSFI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584825
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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