A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv844n223



Internal ID22803812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87483101..87516100hg38UCSC Ensembl
chr10:89242858..89275857hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3833000
hg1933000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6446364, nsv6437435, nsv6451670
Samples
Known GenesMINPP1, MIR4678
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv844n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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