A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv616n209



Internal ID22826691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98916728..98918545hg38UCSC Ensembl
chr14:99383065..99384882hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381818
hg191818
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5851143, nsv5862750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv616n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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