A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478549



Internal ID21136102
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 StatusM
Merged Variants
Supporting Variantsnssv18193793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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