A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850360



Internal ID22625295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10942900..10956502hg38UCSC Ensembl
chr11:10964447..10978049hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813603
hg1913603
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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