A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860237



Internal ID22635172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109486236..109488635hg38UCSC Ensembl
chr13:110138583..110140982hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860237
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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