A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859427



Internal ID22634362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18196939..18200390hg38UCSC Ensembl
chrUn_gl000212:25691..29142hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383452
hg193452
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv504n209
Supporting Variantsnssv17462678, nssv17454618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859427
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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