A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410547



Internal ID21068100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139491948..139493726hg38UCSC Ensembl
chr5:138871533..138873311hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381779
hg191779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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