A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658829



Internal ID21607134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25041168..25041168hg38UCSC Ensembl
chr18:22621132..22621132hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100803
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658829
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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