A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661019



Internal ID21609324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25709575..25709575hg38UCSC Ensembl
chr18:23289539..23289539hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100550
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661019
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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