A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182835



Internal ID20749875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68963501..69012800hg38UCSC Ensembl
chr13:69537633..69586932hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3849300
hg1949300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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