A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479448



Internal ID21137001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69380401..69384600hg38UCSC Ensembl
chr13:69954533..69958732hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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