A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4161n223



Internal ID22807129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158849264..158876326hg38UCSC Ensembl
chr2:159705776..159732838hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3827063
hg1927063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6341226, nsv6344044, nsv6341406, nsv6346835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4161n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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