A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407489



Internal ID21065042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138777588..138811761hg38UCSC Ensembl
chr5:138113277..138147450hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3834174
hg1934174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215059
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407489
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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