A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443810



Internal ID21101363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65499301..65519900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3820600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443810
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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