A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842416



Internal ID22026059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93497717..93497717hg38UCSC Ensembl
chr10:95257474..95257474hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247384
Supporting Variants
Samples
Known GenesCEP55
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842416
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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