A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841955



Internal ID22025598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66157078..66157078hg38UCSC Ensembl
chr10:67916836..67916836hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247177
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841955
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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