A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4125n223



Internal ID22807093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:131338901..131594268hg38UCSC Ensembl
chr2:132096474..132351841hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38255368
hg19255368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6348008, nsv6337331
Samples
Known GenesCCDC74A, LINC01120, LOC150776, LOC401010, MIR4784, MZT2A, RNU6-81P, TUBA3D, WTH3DI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4125n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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