A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570060



Internal ID21518424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26002840..26002907hg38UCSC Ensembl
chr8:25860356..25860423hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142524
SamplesHG02818
Known GenesEBF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570060
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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