A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660632



Internal ID21608937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47982481..47982481hg38UCSC Ensembl
chr18:45508852..45508852hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101238
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660632
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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