A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451296



Internal ID21108849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80652201..80670500hg38UCSC Ensembl
chr9:83267116..83285415hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3818300
hg1918300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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