A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178026



Internal ID20745066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77687015..77693756hg38UCSC Ensembl
chr15:77979357..77986098hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg386742
hg196742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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