A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707097



Internal ID21379373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45789560..45789613hg38UCSC Ensembl
chr3:45831052..45831105hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390465
Supporting Variants
Samples
Known GenesSLC6A20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707097
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.428161


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