A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271261



Internal ID20480479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25218679..25218788hg38UCSC Ensembl
chr22:25614646..25614755hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271261
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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