A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445079



Internal ID21102632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132083598..132090410hg38UCSC Ensembl
chr9:134958985..134965797hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg386813
hg196813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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