A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3677n223



Internal ID22806645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48602527..48622019hg38UCSC Ensembl
chr19:49105784..49125276hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3819493
hg1919493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6523344, nsv6526815
Samples
Known GenesFAM83E, RPL18, SPACA4, SPHK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3677n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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