A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840118



Internal ID22615053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77514760..77517992hg38UCSC Ensembl
chr4:78435914..78439146hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg383233
hg193233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497254
Samples
Known GenesCXCL13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840118
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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