A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv649n223



Internal ID22803617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22309901..22362700hg38UCSC Ensembl
chr10:22598830..22651629hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3852800
hg1952800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6446055, nsv6449826
Samples
Known GenesBMI1, COMMD3, COMMD3-BMI1, SPAG6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv649n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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