A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179760



Internal ID20746800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65639379..66646719hg38UCSC Ensembl
chr13:66213511..67220851hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381007341
hg191007341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495149
Supporting Variants
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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