A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196336



Internal ID20763376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40571086..40573118hg38UCSC Ensembl
chr15:40863285..40865317hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506298
Supporting Variants
Samples
Known GenesRPUSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196336
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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