A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7342n223



Internal ID22810310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52261418..52708295hg38UCSC Ensembl
chr8:53173978..53620855hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38446878
hg19446878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6422900, nsv6426673
Samples
Known GenesFAM150A, RB1CC1, ST18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7342n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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