A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585721



Internal ID21534269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47061025..47061120hg38UCSC Ensembl
chr22:47456921..47457016hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131659
SamplesHG03065
Known GenesTBC1D22A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585721
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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