A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218198



Internal ID20785238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5969721..6445436hg38UCSC Ensembl
chr9:5969721..6445436hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38475716
hg19475716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430844
Supporting Variants
Samples
Known GenesIL33, KIAA2026, MIR4665, RANBP6, TPD52L3, UHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218198
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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