A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1010n209



Internal ID22827085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10481016..10485605hg38UCSC Ensembl
chr19:10591692..10596281hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384590
hg194590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5946988, nsv5937783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1010n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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