A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4037n223



Internal ID22807005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90241801..90306900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3865100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6345112, nsv6342033, nsv6342825, nsv6342415, nsv6353164, nsv6337158, nsv6352681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4037n223
Frequency
Sample Size19652
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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