A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866417



Internal ID22641352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118075757..118128233hg38UCSC Ensembl
chr11:117946472..117998948hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3852477
hg1952477
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464295
Samples
Known GenesTMPRSS4, TMPRSS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866417
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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