A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857536



Internal ID22632471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118947651..118962098hg38UCSC Ensembl
chr11:118818361..118832808hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3814448
hg1914448
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450316
Samples
Known GenesUPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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