A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409880



Internal ID21067433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133936059..133936579hg38UCSC Ensembl
chr5:133271750..133272270hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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