A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855727



Internal ID22630662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115357317..115360754hg38UCSC Ensembl
chr8:116369546..116372983hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg383438
hg193438
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855727
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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