A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840360



Internal ID22615295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112710263..112711362hg38UCSC Ensembl
chr5:112045960..112047059hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493094
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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