A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3852n223



Internal ID22806820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45159446..45915141hg38UCSC Ensembl
chr2:45386585..46142280hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38755696
hg19755696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6340894, nsv6355409
Samples
Known GenesLINC01121, PRKCE, SRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3852n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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