A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183825



Internal ID20750865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95684986..95695304hg38UCSC Ensembl
chr15:96228215..96238533hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3810319
hg1910319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00102


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