A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038475



Internal ID93378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100454549..100509731hg38UCSC Ensembl
chr10:102214306..102269488hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3855183
hg1955183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489745
Supporting Variants
Samples
Known GenesSEC31B, WNT8B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038475
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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