A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653926



Internal ID21602231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35574458..35574458hg38UCSC Ensembl
chr18:33154422..33154422hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100871
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653926
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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