A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660208



Internal ID21608513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9058020..9058020hg38UCSC Ensembl
chr18:9058018..9058018hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103070
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660208
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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