A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193277



Internal ID20760317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95327201..95330100hg38UCSC Ensembl
chr15:95870430..95873329hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00059


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