A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039974



Internal ID94370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102915225..102915260hg38UCSC Ensembl
chr10:104674982..104675017hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551272
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039974
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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