A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035630



Internal ID91501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68826479..68828226hg38UCSC Ensembl
chr10:70586236..70587983hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481604
Supporting Variants
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035630
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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