A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032528



Internal ID89373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17365142..17369544hg38UCSC Ensembl
chr10:17407141..17411543hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384403
hg194403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488841
Supporting Variants
Samples
Known GenesST8SIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032528
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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