A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv599n209



Internal ID22826674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55077962..55085357hg38UCSC Ensembl
chr14:55544680..55552075hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg387396
hg197396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5938092, nsv5931819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv599n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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