A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452091



Internal ID21109644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130599031..130605722hg38UCSC Ensembl
chr9:133474418..133481109hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386692
hg196692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219695
Samples
Known GenesFUBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452091
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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