A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039229



Internal ID93881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114860681..114860732hg38UCSC Ensembl
chr10:116620440..116620491hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409417
Supporting Variants
Samples
Known GenesFAM160B1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039229
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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