A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858208



Internal ID22633143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66658306..66671266hg38UCSC Ensembl
chr11:66425777..66438737hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3812961
hg1912961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459021
Samples
Known GenesRBM4, RBM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858208
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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