A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276855



Internal ID20486073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50307737..50307804hg38UCSC Ensembl
chr22:50746166..50746233hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276855
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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