A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422082



Internal ID21079635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16833047..17018515hg38UCSC Ensembl
chr9:16833045..17018513hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38185469
hg19185469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219417
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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