A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841019



Internal ID22615954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119379321..119382940hg38UCSC Ensembl
chr5:118715016..118718635hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg383620
hg193620
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493771
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841019
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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