A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652535



Internal ID21600840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24175103..24175103hg38UCSC Ensembl
chr18:21755067..21755067hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101079
SamplesHG03486
Known GenesOSBPL1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652535
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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