A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041152



Internal ID95137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115866314..115908371hg38UCSC Ensembl
chr10:117625825..117667882hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3842058
hg1942058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499698
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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