A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841536



Internal ID22616471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159254295..159256346hg38UCSC Ensembl
chr5:158681303..158683354hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382052
hg192052
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496958, nssv17496959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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