A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2190n209



Internal ID22828265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122839624..122844723hg38UCSC Ensembl
chr9:125601903..125607002hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5867123, nsv5865769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2190n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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