A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633890



Internal ID21582195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85558036..85558036hg38UCSC Ensembl
chr10:87317793..87317793hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071523
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633890
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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