A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627386



Internal ID21575691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129090559..129090559hg38UCSC Ensembl
chr10:130888823..130888823hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068735
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627386
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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