A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485087



Internal ID21142640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66801198..66892796hg38UCSC Ensembl
chr13:67375330..67466928hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3891599
hg1991599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191493
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485087
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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