A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586886



Internal ID21535443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28413887..28415051hg38UCSC Ensembl
chr18:25993851..25995015hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100678
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586886
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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