A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403811



Internal ID21061364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95952872..96356331hg38UCSC Ensembl
chr5:95288576..95692035hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38403460
hg19403460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215428
Samples
Known GenesELL2, MIR583
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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