A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405111



Internal ID21062664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85294401..85325500hg38UCSC Ensembl
chr5:84590219..84621318hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3831100
hg1931100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5800n223
Supporting Variantsnssv18214279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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