A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3059n223



Internal ID22806027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22088595..22573535hg38UCSC Ensembl
chr17:21666609..22072862hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38484941
hg19406254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6497015, nsv6505032
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3059n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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