A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854831



Internal ID22629766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33792948..33803997hg38UCSC Ensembl
chr11:33814494..33825543hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811050
hg1911050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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