A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628732



Internal ID21577037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126482594..126482594hg38UCSC Ensembl
chr8:127494839..127494839hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139886
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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