A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636322



Internal ID21584627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80072352..80072352hg38UCSC Ensembl
chr8:80984587..80984587hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140370, nssv17144728
SamplesHG03486, HG03371
Known GenesTPD52
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636322
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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