A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850196



Internal ID22625131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92366301..92368443hg38UCSC Ensembl
chr11:92099467..92101609hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg382143
hg192143
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458181
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850196
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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