A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2191n209



Internal ID22828266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124894913..124895830hg38UCSC Ensembl
chr9:127657192..127658109hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5915985, nsv5925981
Samples
Known GenesGOLGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2191n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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