A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862250



Internal ID22637185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126394393..126397477hg38UCSC Ensembl
chr11:126264288..126267372hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454350
Samples
Known GenesST3GAL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862250
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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