A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv64n209



Internal ID22826139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123341168..123807183hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38466016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5883306, nsv5884816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv64n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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