A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187520



Internal ID20754560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24202186..24509830hg38UCSC Ensembl
chr15:24447333..24754977hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38307645
hg19307645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187520
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00022


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