A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859731



Internal ID22634666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6482190..6484239hg38UCSC Ensembl
chr9:6482190..6484239hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382050
hg192050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513985
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859731
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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