A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644022



Internal ID21592327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106285864..106285864hg38UCSC Ensembl
chr8:107298092..107298092hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157762
SamplesNA12878
Known GenesOXR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644022
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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