A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380384



Internal ID21037937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39262225..39263105hg38UCSC Ensembl
chr5:39262327..39263207hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213457
Samples
Known GenesFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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