A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854536



Internal ID22629471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92718456..92724506hg38UCSC Ensembl
chr11:92451622..92457672hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457393
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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