A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482280



Internal ID21139833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81527891..81586240hg38UCSC Ensembl
chr13:82102026..82160375hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3858350
hg1958350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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