A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447784



Internal ID21105337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41238601..41364900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38126300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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