A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404583



Internal ID21062136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114920001..114933500hg38UCSC Ensembl
chr5:114255698..114269197hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5901n223
Supporting Variantsnssv18212455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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