A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv66n209



Internal ID22826141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123412023..124443865hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381031843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5878861, nsv5876840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv66n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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