A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545130



Internal ID21869485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14435294..14435347hg38UCSC Ensembl
chr3:14476802..14476855hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991417
Supporting Variants
Samples
Known GenesSLC6A6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545130
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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