A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622924



Internal ID21814971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89545520..89545611hg38UCSC Ensembl
chr16:89611928..89612019hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028342
Supporting Variants
Samples
Known GenesSPG7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622924
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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