A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219028



Internal ID20786068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46995567..47006450hg38UCSC Ensembl
chr6:46963304..46974187hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3810884
hg1910884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412902
Supporting Variants
Samples
Known GenesGPR110
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219028
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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