A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194667



Internal ID20761707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60286407..60299641hg38UCSC Ensembl
chr13:60860541..60873775hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3813235
hg1913235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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