A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887092



Internal ID22662084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22474155..22487586hg38UCSC Ensembl
chr18:20054118..20067549hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3813432
hg1913432
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887092
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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