A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863303



Internal ID22638238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18504789..18506819hg38UCSC Ensembl
chr11:18526336..18528366hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382031
hg192031
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451201
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863303
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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