A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219354



Internal ID20786394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77654401..77666900hg38UCSC Ensembl
chr9:80269317..80281816hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450256
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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