A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228469



Internal ID20795509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89391260..89424257hg38UCSC Ensembl
chr9:92006175..92039172hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3832998
hg1932998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452794
Supporting Variants
Samples
Known GenesSEMA4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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