A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193095



Internal ID20760135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114249482..114314400hg38UCSC Ensembl
chr13:115014957..115079875hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3864919
hg1964919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477363
Supporting Variants
Samples
Known GenesCDC16, UPF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193095
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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