A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866265



Internal ID22641200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115212220..115215905hg38UCSC Ensembl
chr8:116224449..116228134hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg383686
hg193686
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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