A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706392



Internal ID21378668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11557349..11557419hg38UCSC Ensembl
chr19:11668164..11668234hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392281
Supporting Variants
Samples
Known GenesELOF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706392
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0114943


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