A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657672



Internal ID21605977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61897584..61897584hg38UCSC Ensembl
chr18:59564817..59564817hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101731
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657672
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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