A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656045



Internal ID21604350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62691283..62691283hg38UCSC Ensembl
chr18:60358516..60358516hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101565
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656045
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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