A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428397



Internal ID21085950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24485156..25373713hg38UCSC Ensembl
chr9:24485154..25373711hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38888558
hg19888558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225162
Samples
Known GenesIZUMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428397
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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