A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628165



Internal ID21576470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26680363..26680363hg38UCSC Ensembl
chr8:26537880..26537880hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155821
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628165
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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