A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222298



Internal ID20789338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83905998..84000328hg38UCSC Ensembl
chr9:86520913..86615243hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3894331
hg1994331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451907
Supporting Variants
Samples
Known GenesC9orf64, HNRNPK, KIF27, MIR7-1, RMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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