A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3823n223



Internal ID22806791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32271928..32374707hg38UCSC Ensembl
chr2:32496997..32599775hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38102780
hg19102779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6350611, nsv6348824
Samples
Known GenesBIRC6, YIPF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3823n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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