A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219884



Internal ID20786924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139956601..139985700hg38UCSC Ensembl
chr8:140968899..140995910hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3829100
hg1927012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421746
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00012


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