A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639598



Internal ID21587903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129773308..129773308hg38UCSC Ensembl
chr10:131571572..131571572hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066821
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639598
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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