A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1647n209



Internal ID22827722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2862496..2863086hg38UCSC Ensembl
chr5:2862610..2863200hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5896102, nsv5899872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1647n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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