A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653819



Internal ID21602124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24435871..24435871hg38UCSC Ensembl
chr18:22015835..22015835hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101083
SamplesHG00513
Known GenesIMPACT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653819
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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