A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv260n209



Internal ID22826335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58832259..59011722hg38UCSC Ensembl
chr11:58599732..58779195hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38179464
hg19179464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5908645, nsv5918762
Samples
Known GenesGLYATL1, GLYATL2, LOC283194
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv260n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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