A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495149



Internal ID21152702
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 StatusM
Merged Variants
Supporting Variantsnssv18179760
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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