A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443353



Internal ID21100906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41753501..41811400hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3857900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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