A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228276



Internal ID20795316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94999701..95016900hg38UCSC Ensembl
chr9:97761983..97779182hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3817200
hg1917200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442259
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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