A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208807



Internal ID20775847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33417750..33449589hg38UCSC Ensembl
chr2:33642817..33674656hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3831840
hg1931840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346386
Supporting Variants
Samples
Known GenesRASGRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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