A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220143



Internal ID20787183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94756962..94781655hg38UCSC Ensembl
chr9:97519244..97543937hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3824694
hg1924694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454266
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220143
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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