A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178765



Internal ID20745805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114184731..114296297hg38UCSC Ensembl
chr13:114950206..115061772hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38111567
hg19111567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483392
Supporting Variants
Samples
Known GenesCDC16, UPF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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