A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646791



Internal ID21838838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25999515..25999576hg38UCSC Ensembl
chr22:26395481..26395542hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054044
Supporting Variants
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646791
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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