A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525740



Internal ID21850098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11249944..11250066hg38UCSC Ensembl
chr1:11310001..11310123hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980608
Supporting Variants
Samples
Known GenesMTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525740
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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