A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193793



Internal ID20760833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69390644..69415406hg38UCSC Ensembl
chr13:69964776..69989538hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3824763
hg1924763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193793
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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