A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv882n223



Internal ID22803850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104783726..106005877hg38UCSC Ensembl
chr10:106543484..107765635hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381222152
hg191222152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6451417, nsv6440655
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv882n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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