A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039922



Internal ID94336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102425716..102425750hg38UCSC Ensembl
chr10:104185473..104185507hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554237
Supporting Variants
Samples
Known GenesCUEDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039922
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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