A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843368



Internal ID22618303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6080033..6082282hg38UCSC Ensembl
chr5:6080146..6082395hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497453, nssv17497452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843368
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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