A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv120n209



Internal ID22826195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222376875..222377863hg38UCSC Ensembl
chr1:222550217..222551205hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5881890, nsv5871932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv120n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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