A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261168



Internal ID20470386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48337288..48337361hg38UCSC Ensembl
chr22:48733100..48733173hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261168
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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