A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039161



Internal ID93846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113679225..113732415hg38UCSC Ensembl
chr10:115438984..115492174hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3853191
hg1953191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505924
Supporting Variants
Samples
Known GenesCASP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039161
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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