A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141794



Internal ID340992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65385061..65397123hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3812063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141794
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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