A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152959



Internal ID21505947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106338293..106339212hg38UCSC Ensembl
chr8:107350521..107351440hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573161
Supporting Variants
SamplesNA19983
Known GenesOXR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152959
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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