A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869819



Internal ID22644754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80028894..80031393hg38UCSC Ensembl
chr18:77788894..77791393hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479898, nssv17479897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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