A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855364



Internal ID22630299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114284182..114287910hg38UCSC Ensembl
chr8:115296411..115300139hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg383729
hg193729
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505558, nssv17505557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855364
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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