A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486428



Internal ID21143981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36035115..36057823hg38UCSC Ensembl
chr13:36609252..36631960hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3822709
hg1922709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196503
Samples
Known GenesDCLK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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