A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591350



Internal ID21539925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24729467..24729519hg38UCSC Ensembl
chr18:22309431..22309483hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100792
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591350
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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