A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033971



Internal ID90346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62089908..62089925hg38UCSC Ensembl
chr10:63849667..63849684hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg383185
hg193185
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559311
Supporting Variants
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033971
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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