A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486809



Internal ID21144362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86028857..86092997hg38UCSC Ensembl
chr13:86602992..86667132hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3864141
hg1964141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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