A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637365



Internal ID21585670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126947813..126947813hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383694
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067670
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637365
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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