A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4657n223



Internal ID22807625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25238496..25470673hg38UCSC Ensembl
chr22:25634463..25866640hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38232178
hg19232178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6549464, nsv6545392, nsv6554036, nsv6553831
Samples
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4657n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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