A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033468



Internal ID90000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29082874..29296506hg38UCSC Ensembl
chr10:29371803..29585435hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38213633
hg19213633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483840
Supporting Variants
Samples
Known GenesLYZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033468
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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