A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842793



Internal ID22617728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60414495..60473581hg38UCSC Ensembl
chr5:59710322..59769408hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3859087
hg1959087
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497446
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842793
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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