A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867047



Internal ID22641982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23276614..23277963hg38UCSC Ensembl
chr8:23134127..23135476hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867047
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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