A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294690



Internal ID20503908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190113796..190113977hg38UCSC Ensembl
chr3:189831585..189831766hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747248
Supporting Variants
Samples
Known GenesLEPREL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294690
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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