A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370513



Internal ID22596182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87127943..87146705hg38UCSC Ensembl
chr15:87671174..87689936hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818763
hg1918763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370513
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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