A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638340



Internal ID21586645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115776593..115776593hg38UCSC Ensembl
chr10:117536104..117536104hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067525
SamplesNA19239
Known GenesATRNL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638340
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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