A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661455



Internal ID21609760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:192071..192071hg38UCSC Ensembl
chr18:192071..192071hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100545
SamplesHG00512
Known GenesUSP14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661455
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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