A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624635



Internal ID21572940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106604268..106604268hg38UCSC Ensembl
chr8:107616496..107616496hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142402
SamplesNA18939
Known GenesOXR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624635
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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