A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035633



Internal ID91502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68844791..68847447hg38UCSC Ensembl
chr10:70604547..70607203hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382657
hg192657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143771
Supporting Variants
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01827


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