A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182088



Internal ID20749128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67116460..67276647hg38UCSC Ensembl
chr13:67690592..67850779hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38160188
hg19160188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478406
Supporting Variants
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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