A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2180n209



Internal ID22828255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110517513..110523702hg38UCSC Ensembl
chr9:113279793..113285982hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg386190
hg196190
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5857995, nsv5867104
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2180n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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