A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488841



Internal ID266134
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 StatusM
Merged Variantsdgv42n206
Supporting Variantsnssv17032528
Samples
Known GenesST8SIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488841
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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