A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859826



Internal ID22634761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103302691..103354962hg38UCSC Ensembl
chr13:103955041..104007312hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3852272
hg1952272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859826
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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